Weekly Recall Recap

NewerOlder

2026-04-13 to 2026-04-19

123
Recalls
1,571,127
Units
19
Injuries
0
Deaths

Sources: NHTSA, CPSC, FDA_DEVICE, FDA_DRUG, FDA_FOOD

Other Recalls

NHTSA2026-04-1736 units
Improperly Installed Front End Radar
Altec Industries, Inc.

While driving, the brakes may activate unexpectedly without the driver's input, increasing the risk of a crash.

NHTSA2026-04-17103 units
Improperly Tightened Windshield Wiper Blade Assemblies
Blue Bird Body Company

Loose fasteners may cause the windshield wipers to become inoperative, reducing visibility and increasing the risk of a crash.

NHTSA2026-04-176 units
Improperly Tightened Windshield Wiper Blade Assemblies
Blue Bird Body Company

Loose fasteners may cause the windshield wipers to become inoperative, reducing visibility and increasing the risk of a crash.

NHTSA2026-04-1640 units
Inoperative Emergency Stop Switch
Altec Industries, Inc.

An inoperative emergency stop switch increases the risk of injury.

CPSC2026-04-16
Sweetcrispy Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards

The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution hazards.

NHTSA2026-04-162,689 units
Engine Failure May Cause Fire or Loss of Drive Power
Chrysler (FCA US, LLC)

A loss of drive power increases the risk of a crash, and a vehicle fire increases the risk of injury.

CPSC2026-04-16
JC Sales Recalls Lil' Buddies Pet Laser Toys Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Consumer Products with Button Cell Batteries

The Montessori toy sets contain an airplane shaped teething toy that has tentacle ends that can pose a choking hazard to young children. The toys also violate the teething toy provision of the mandatory standard for children's toys.

CPSC2026-04-16
Generac Power Systems Recalls Portable Generators Due to Risk of Serious Injury or Death from Burn and Fire Hazards

When first filling the recalled generator with gasoline, fuel can leak from the carburetor, posing a risk of serious injury or death from fire or burn hazard. Consumers with generators that have previously been filled with enough gasoline to move the gauge off "E," or have been used without any gasoline leakage, can continue to be used.

CPSC2026-04-16
Free-Standing Professional Gas Ranges Recalled Due to Risk of Burn Hazard; Manufactured by Fisher & Paykel
Fisher & Paykel Appliances (Thailand) Co., Ltd, of Thailand

The ovens in the ranges can experience a delayed ignition, causing gas to accumulate and the oven door to open from combustion, posing a burn hazard to users.

CPSC2026-04-16
Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Imported by BAYOTAK USA

The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution hazards.

CPSC2026-04-16
nvyue Magic Pocket Staffs Recalled Due to Projectile and Laceration Hazards; Imported by Xingwenfeng

The protective pin mechanism on the Magic Pocket Staffs can fail to prevent unintentional expansion, posing serious projectile and laceration hazards. Even when engaged, the expansion occurs too rapidly for consumers to react, leaving virtually no opportunity for protection.

NHTSA2026-04-161,217 units
Do Not Drive: Loss of Steering Control from Loose or Missing Fasteners
Roush Performance Products, Inc.

Loose or missing fasteners can cause a loss of vehicle steering and control, increasing the risk of a crash.

CPSC2026-04-16
ZMC Group Recalls LED Finger Beam Lights Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys

The recalled toys violate the mandatory safety standard for children's toys because the toy contains button cell batteries that can be easily accessed by children. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.

CPSC2026-04-16
Fengrong Tool Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards

The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution hazards.

CPSC2026-04-16
Mini Round Toddler Trampolines Recalled Due to Strangulation Hazard; Risk of Serious Injury or Death; Manufactured by SEGMART
Shenzhen Segmart Technology Electronics Co., Ltd., of China

Young children can become entangled in the straps of the hammock, punching bag and hand ring accessories, posing a strangulation hazard, which can result in serious injury or death.

CPSC2026-04-16
Macy's Recalls Arch Studio Tea Kettles Due to Risk of Serious Injury from Burn Hazard

The tea kettles' handle can detach during use when heated, posing a risk of serious injury from burn hazard.

CPSC2026-04-16
Apex Gaming PCs Recalls Manik and Apex-branded ATX Computer Power Supplies Due to Risk of Serious Injury or Death from Electrical Shock and Electrocution Hazards

The units lack a permanent, on-product warning label identifying potential electrical shock and electrocution hazards, posing a risk of serious injury or death if the unit is opened or disassembled.

CPSC2026-04-16
ATOYUS Children's Activity Cubes Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Small Parts Ban and Mandatory Standard for Toys; Sold on Amazon by Melofaver US

The recalled toys violate the small parts ban because the toys are intended for children under three and the toys' xylophone screws and clock hands can detach. In addition, the toys violate the mandatory safety standard for children's toys because the mallets have spherical ends, posing a choking hazard.

CPSC2026-04-16
Le Hao Tool Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards

The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution hazards.

CPSC2026-04-16
Agiiman Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards

The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution.

CPSC2026-04-16
Montessori Toy Sets Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Mandatory Standard for Teething Toys; Sold on Amazon by SpringFlower

The Montessori toy sets contain an airplane shaped teething toy that has tentacle ends that can pose a choking hazard to young children. The toys also violate the teething toy provision of the mandatory standard for children's toys.

CPSC2026-04-16
Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by ZOLIQUEX
ZOLIQUEX, of China

The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning labels.

CPSC2026-04-16
Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Imported by Patoolio Direct

The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution hazards.

NHTSA2026-04-166,605 units
Loss of Electronic Stability Control/FMVSS 126
Chrysler (FCA US, LLC)

A loss of electronic stability control increases the risk of a crash.

CPSC2026-04-16
Fun and Function Recalls Children's Metal Multi-Point Swing Frames Due to Risk of Injury from Fall Hazard

The swing frames can crack or break during use, posing a fall hazard, which can result in injury.

CPSC2026-04-16
Sanlebi Pet Vet Playsets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by Letokids
Guangzhou Letao Keji Youxiangongsi, doing business as Letokids, of China

The Pet Vet Playset violates the mandatory standard for toys because the button cell batteries in the nail grinder and otoscope can be easily accessed by children.

NHTSA2026-04-1520 units
Missing Side Reflectors/FMVSS 108
Winnebago Industries, Inc.

Missing reflectors can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash.

FDA Device2026-04-15
FDA Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syring
Medline Industries, LP

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

FDA Device2026-04-15
FDA Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syring
Medline Industries, LP

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

FDA Device2026-04-15
FDA Recall: COOK MEDICAL Multipurpose Drainage Catheter: Reference Part Number ULT8.5-38-25-P-CLMS-8-RH-FS, Ord
Cook Incorporated

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

FDA Device2026-04-15
FDA Recall: COOK MEDICAL Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set: Reference Part Number C-
Cook Incorporated

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

FDA Device2026-04-15
FDA Recall: Tornier HRS Max parts: 1. TORNIER HRS Max Tuberosity Body Lat Coat, Small, Cat. No. ARS1041101
Tornier, Inc

Affected products were incorrectly labeled as Tornier HRS Max products. These parts are compatible with the Tornier HRS system only, and are incompatible with the Tornier HRS Max system.

FDA Device2026-04-15
FDA Recall: See Luer Cap Set, MPC-130, set, administration, intravascular
Molded Products Inc

Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the threaded sleeve not being engaged and becoming un-attached.

FDA Device2026-04-15
FDA Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syring
Medline Industries, LP

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

FDA Device2026-04-15
FDA Recall: MicroScan Neg MIC 3J REF C54814
Beckman Coulter, Inc.

Due to a manufacturing issue - missing a drug in well 4/4 but contain double the amount of antibiotics

FDA Drug2026-04-15
FDA Recall: 0.9% Sodium Chloride Injection, USP, 900 mg per 100 mL (9 mg per mL) 100 mL in a Single Dose freefle
Fresenius Kabi USA, LLC

Lack of Assurance of Sterility

FDA Device2026-04-15
FDA Recall: COOK MEDICAL Thal-Quick Chest Tube Tray: Reference Part Number C-TQTSY-3200, Order Number G07242
Cook Incorporated

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

FDA Device2026-04-15
FDA Recall: NAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027;
Medline Industries, LP

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

FDA Device2026-04-15
FDA Recall: COOK MEDICAL Approach CTO-6 Micro Wire Guide, Reference Part Number CMW-14-190-6G, Order Number G507
Cook Incorporated

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

FDA Device2026-04-15
FDA Recall: ARTIS pheno and ARTIS Icono biplane, floor and ceiling. Model Numbers 10849000, 11327600, 11328100,
Siemens Medical Solutions USA, Inc

During patient examinations, the system may sporadically display a major increase of the x-ray dose applied to the patient. Despite the reported dose showing significantly higher, the actual applied x-ray dose levels are in accordance with the system settings and imaging conditions, as well as the applicable regulatory requirements.

FDA Device2026-04-15
FDA Recall: COOK MEDICAL Spectrum¿ Central Venous Tray: Reference Part Number C-UQLMYJ-1001J-RSC-ABRM-HC-FST-A-
Cook Incorporated

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

FDA Device2026-04-15
FDA Recall: Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5
Stryker Sustainability Solutions

Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.

FDA Device2026-04-15
FDA Recall: COOK MEDICAL Cook Staged Extubation Set: Reference Part Number C-CAE-14.0-83-EXTU, Order Number G24
Cook Incorporated

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

FDA Device2026-04-15
FDA Recall: COOK MEDICAL Ciaglia Blue Rhino Percutaneous Tracheostomy Introducer Set: Reference Part Number C-P
Cook Incorporated

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

FDA Device2026-04-15
FDA Recall: NAMIC Angiographic Control Syringe, labeled as follows: 1. SYRINGE,7ML,TR/FR,RA,W/RES,-,P/G, Medl
Medline Industries, LP

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

FDA Device2026-04-15
FDA Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syring
Medline Industries, LP

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

FDA Drug2026-04-15
FDA Recall: Lanreotide Injection, 120 mg*/0.5 mL, Box contains 1 Pre-filled syringe and 1 safety needle, Single
Cipla USA, Inc.

Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.

FDA Drug2026-04-15
FDA Recall: 0.9% Sodium Chloride Injection, USP 900 mg per 100 mL (9 mg per mL), 1,000 mL in a Single Dose freef
Fresenius Kabi USA, LLC

Lack of Assurance of Sterility

FDA Device2026-04-15
FDA Recall: COOK MEDICAL Spectrum¿ Central Venous Catheter Set: Reference Part Number C-UDLM-401J-ABRM-HC, Orde
Cook Incorporated

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

FDA Drug2026-04-15
FDA Recall: 0.9% Sodium Chloride Injection, USP, 900 mg per 100 mL (9 mg per mL) 250 mL in a Single Dose freefle
Fresenius Kabi USA, LLC

Lack of Assurance of Sterility

FDA Drug2026-04-15
FDA Recall: 0.9% Sodium Chloride Injection, USP, 50 mL x60, Becton, Dickson and Company, 1 Beckton Drive, Frankl
Fresenius Kabi USA, LLC

Lack of Assurance of Sterility

FDA Drug2026-04-15
FDA Recall: 0.9% Sodium Chloride Injection, USP 0.9% (450 mg per 50 mL) (9 mg per mL) 50 mL, Rx only, Fresenius
Fresenius Kabi USA, LLC

Lack of Assurance of Sterility

FDA Drug2026-04-15
FDA Recall: norepinephrine Bitartrate,16mg per 250mL 0.9% Sodium Chloride Injection USP, Fagron Sterile Services
Fagron Compounding Services

Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port

FDA Drug2026-04-15
FDA Recall: Artificial Tears Lubricant Eye Drops (glycerin 0.2%, hypromellose 0.2%, polyethylene glycol 400 1%),
Preferred Pharmaceuticals, Inc.

Lack of Assurance of Sterility

FDA Drug2026-04-15
FDA Recall: Xanax XR, alprazolam, extended-release tablets, 3 mg, 60 Tablets bottles, Rx only, Distributed by: V
Viatris, Inc.

Failed Dissolution Specifications

FDA Drug2026-04-15
FDA Recall: 0.9% Sodium Chloride Injection, USP, 900 mg per 100 mL (9 mg per mL) 1,000 mL in a Single Dose freef
Fresenius Kabi USA, LLC

Lack of Assurance of Sterility

FDA Drug2026-04-15
FDA Recall: 5% Dextrose Injection, USP 5 g per 100 mL (50 mg per mL) 100 mL in a 100 mL freeflex bag, Fresenius
Fresenius Kabi USA, LLC

Lack of Assurance of Sterility

FDA Drug2026-04-15
FDA Recall: 5% Dextrose Injection, USP 12.5 g per 250 mL (50 mg per mL) 250 mL in a 250 mL freeflex bag, Freseni
Fresenius Kabi USA, LLC

Lack of Assurance of Sterility

FDA Drug2026-04-15
FDA Recall: norepinephrine Bitartrate, 32mg per 250mL 0.9% Sodium Chloride Injection USP, Fagron Sterile Service
Fagron Compounding Services

Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port

FDA Drug2026-04-15
FDA Recall: Clonidine Transdermal System, USP, 0.3 mg/day, supplied in cartons of 4 Systems and 4 Adhesive Cover
Teva Pharmaceuticals USA, Inc

CGMP Deviations: use of an unapproved raw material

FDA Drug2026-04-15
FDA Recall: 5% Dextrose Injection, USP 2.5 g per 50 mL (50 mg per mL) 50 mL in a 100 mL freeflex bag, Fresenius
Fresenius Kabi USA, LLC

Lack of Assurance of Sterility

FDA Drug2026-04-15
FDA Recall: Lanreotide Injection, 120 mg/0.5 mL, Box contains 1 Pre-filled syringe, Single dose only, Rx Only, M
Cipla USA, Inc.

Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.

FDA Drug2026-04-15
FDA Recall: Vancomycin HCI, 1.25 grams added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Servi
Fagron Compounding Services

Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port

FDA Drug2026-04-15
FDA Recall: 0.9% Sodium Chloride Injection, USP, (4,500 mg per 500 mL) (9 mg per mL) 500 mL in a 500 mL freeflex
Fresenius Kabi USA, LLC

Lack of Assurance of Sterility

FDA Drug2026-04-15
FDA Recall: 0.9% Sodium Chloride Injection, USP, 0.9% (900 mg per 100 mL) (9 mg per mL) 100 mL in a 100 mL freef
Fresenius Kabi USA, LLC

Lack of Assurance of Sterility

FDA Drug2026-04-15
FDA Recall: 0.9% Sodium Chloride Injection, USP 900 mg per 100 mL (9 mg per mL) 500 mL in a Single Dose freeflex
Fresenius Kabi USA, LLC

Lack of Assurance of Sterility

FDA Drug2026-04-15
FDA Recall: 0.9% Sodium Chloride Injection, USP, (2,250 mg per 250 mL) (9 mg per mL) 250 mL in a 250 mL freeflex
Fresenius Kabi USA, LLC

Lack of Assurance of Sterility

FDA Drug2026-04-15
FDA Recall: Vancomycin HCI, 1.5 grams added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Servic
Fagron Compounding Services

Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port

FDA Food2026-04-15
FDA Recall: ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich, perishable, Keep Refrigerated, plastic clams
F&S Fresh Foods, Inc.

Undeclared sesame. Sandwich contains visible sesame but label does not declare sesame.

FDA Food2026-04-15
FDA Recall: Boner Bears Honey Male Enhancement 100% Wildflower Honey, total of 15 pouches per box, Net Wt 15 G e
Pure Vitamins and Natural Supplements, LLC

FDA analysis revealed the presence of undeclared sildenafil and Tadalafil

FDA Food2026-04-15
FDA Recall: Zarlengo's Chocolate Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups a
Zarlengo Italian Ice

Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.

FDA Food2026-04-15
FDA Recall: Fresh Cantaloupe (Whole, Fresh), brand name Ayco, wrapped in food safe plastic bags packed in corrug
AYCO FARMS INC

Potential Salmonella Contamination

NHTSA2026-04-1555 units
Block Heater May Overheat and Cause Fire
Ford Motor Company

An overheated engine block heater can increase the risk of a fire.

FDA Food2026-04-15
FDA Recall: DADI NONGFU DRIED SALT CHILLI VEGETABLE(S); Ingredients: Radish, chili, roasted sesame, prickly ash,
MEI YU CHENG DA TRADING INC

Products contain banned sweetener: cyclamates.

FDA Device2026-04-15
FDA Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syring
Medline Industries, LP

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

FDA Device2026-04-15
FDA Recall: B.R.A.H.M.S PlGF Plus KRYPTOR, Catalog Number: 859075N. in vitro diagnostic test for Placental Grow
Brahms GmbH

Customers have observed quality control values out of range at the lowest quality control level (QC Level 1) for the PIGF assay which require troubleshooting steps to resolve. If Quality Controls are not performed according to the Instructions for Use, the underestimation of QC1 may go undetected and could contribute to falsely elevated sFlt-1/PlGF ratio results. A falsely elevated sFlt-1/PlGF ratio may result in a higher-risk classification for progression to preeclampsia with severe features potentially leading to intensified clinical monitoring.

FDA Device2026-04-15
FDA Recall: XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number X073-6555-DL.
XTANT Medical Holdings, Inc

Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is.

FDA Device2026-04-15
FDA Recall: COOK MEDICAL Approach CTO-18 Micro Wire Guide, Reference Part Number CMW-14-190-18G, Order Number G5
Cook Incorporated

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

FDA Device2026-04-15
FDA Recall: NAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 700750
Medline Industries, LP

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

FDA Device2026-04-15
FDA Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syring
Medline Industries, LP

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

FDA Device2026-04-15
FDA Recall: COOK MEDICAL Blue Rhino¿ G2-Multi Percutaneous Tracheostomy Introducer Tray: Reference Part Number
Cook Incorporated

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

FDA Device2026-04-15
FDA Recall: COOK MEDICAL Cook¿ Spectrum¿ Central Venous Catheter Tray: Reference Part Number C-UTLMY-701J-ABRM-
Cook Incorporated

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

FDA Device2026-04-15
FDA Recall: COOK MEDICAL Wayne Pneumothorax Set: Reference Part Number C-UTPT-1020-WAYNE-IMH, Order Number G565
Cook Incorporated

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

FDA Drug2026-04-15
FDA Recall: Isotretinoin Capsules, USP, 40 mg, 10 count Prescription Pacs, Rx only, Manufactured for: Teva Pharm
Teva Pharmaceuticals USA, Inc

Superpotent and Subpotent

FDA Device2026-04-15
FDA Recall: COOK MEDICAL Cook¿ Strange Bile Duct Stone Exploration Set: Reference Part Number C-CSRC-7.5D-40-ST
Cook Incorporated

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

FDA Drug2026-04-15
FDA Recall: GE Healthcare Omnipaque (iohexol) Injection, 350 mg/mL (64.7%), Rx Only, Distributed by: GE Healthca
GE Healthcare Ireland Limited

Presence of particulate matter

FDA Device2026-04-15
FDA Recall: Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set: Reference Part Number C-TCCSB-500-UN
Cook Incorporated

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

FDA Food2026-04-15
FDA Recall: Red Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch. D
Pure Vitamins and Natural Supplements, LLC

FDA analysis revealed the presence of undeclared sildenafil

FDA Device2026-04-15
FDA Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syring
Medline Industries, LP

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

FDA Device2026-04-15
FDA Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syring
Medline Industries, LP

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

FDA Device2026-04-15
FDA Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syring
Medline Industries, LP

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

FDA Device2026-04-15
FDA Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syring
Medline Industries, LP

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

FDA Device2026-04-15
FDA Recall: COOK MEDICAL Approach CTO-12 Micro Wire Guide: Reference Part Number CMW-14-190-12G, Order Number
Cook Incorporated

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

FDA Device2026-04-15
FDA Recall: COOK MEDICAL NCompass¿ Nitinol Stone Extractor: Reference Part Number C-NTSE-2.4-115-NC3, Order Num
Cook Incorporated

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

FDA Device2026-04-15
FDA Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syring
Medline Industries, LP

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

FDA Device2026-04-15
FDA Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syring
Medline Industries, LP

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

FDA Food2026-04-15
FDA Recall: Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids, isoquercitrin, and bromelain)100 count bot
Blueroot Health, Inc.

Contains undeclared egg, soy, and hazelnut

FDA Food2026-04-15
FDA Recall: Blue Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch.
Pure Vitamins and Natural Supplements, LLC

FDA analysis revealed the presence of undeclared sildenafil

FDA Food2026-04-15
FDA Recall: Zarlengo's Chocolate Chocolate Chip Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups,
Zarlengo Italian Ice

Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.

FDA Food2026-04-15
FDA Recall: Zarlengo's Double Dark Chocolate Gelato packaged in 1 Gallon bucket/pail - white round food and free
Zarlengo Italian Ice

Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.

FDA Device2026-04-15
FDA Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syring
Medline Industries, LP

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

FDA Device2026-04-15
FDA Recall: NAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027;
Medline Industries, LP

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

FDA Device2026-04-15
FDA Recall: COOK MEDICAL Wayne Pneumothorax Tray: Reference Part Number C-UTPTY-1400-WAYNE-112497-IMH, Order Nu
Cook Incorporated

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

FDA Drug2026-04-15
FDA Recall: Vancomycin HCL, 1 gram added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services,
Fagron Compounding Services

Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port

FDA Drug2026-04-15
FDA Recall: GE Healthcare Omnipaque (iohexol) Injection, 300 mg/mL (64.7%), Rx Only, Distributed by: GE Healthca
GE Healthcare Ireland Limited

Presence of particulate matter

FDA Drug2026-04-15
FDA Recall: Isotretinoin Capsules, USP, 30 mg, Rx Only, 10 count Prescription Pack, Manufactured for: Teva Pharm
Teva Pharmaceuticals USA, Inc

Superpotent and Subpotent

FDA Device2026-04-15
FDA Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syring
Medline Industries, LP

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

FDA Food2026-04-15
FDA Recall: Olive Skewers individually wrapped and packaged in clear plastic bag; 500g; INGREDIENTS: Olive, edib
MEI YU CHENG DA TRADING INC

Products contain banned sweetener: cyclamates.

FDA Drug2026-04-15
FDA Recall: 0.45% Sodium Chloride Injection, USP, 1.125 grams per 250 mL (4.5 mg per mL), 250 mL in a 250 mL fre
Fresenius Kabi USA, LLC

Lack of Assurance of Sterility

FDA Drug2026-04-15
FDA Recall: Clonidine Transdermal System, USP, 0.2 mg/day, supplied in cartons of 4 Systems and 4 Adhesive Cover
Teva Pharmaceuticals USA, Inc

CGMP Deviations: use of an unapproved raw material

FDA Food2026-04-15
FDA Recall: Riverence Smoked Trout Dip, net wt. 7oz. Product is perishable, refrigerated, packaged in plastic tu
Riverence Provisions LLC

Label declares cream cheese but does not declare milk

FDA Drug2026-04-15
FDA Recall: Clonidine Transdermal System, USP, 0.1 mg/day, supplied in cartons of 4 Systems and 4 Adhesive Cover
Teva Pharmaceuticals USA, Inc

CGMP Deviations: use of an unapproved raw material

FDA Device2026-04-15
FDA Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syring
Medline Industries, LP

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

FDA Device2026-04-15
FDA Recall: Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor
Spacelabs Healthcare, Inc.

Multi-parameter command module has a circuit board issue and when in Auto mode, Cardiac Output (CO) measurement may activate early, resulting in Bad Curve error with no CO measurement or Irregular Curve error with CO measurement not automatically excluded, which may result in inaccurate readings, or the need of additional readings, which may lead to delayed care and/or fluid overload.

FDA Food2026-04-15
FDA Recall: Crab Cakes various sizes sold to food service
Connecticut Crab Company LLC

May be temperature abused, which may result in growth of Clostridium botulinum

FDA Device2026-04-15
FDA Recall: COOK MEDICAL Arterial Pressure Monitoring Tray, Reference Part Number APMY-2.5-15-0-2.5 , Order Numb
Cook Incorporated

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

FDA Device2026-04-15
FDA Recall: MicroScan Neg Multidrug Resistant MIC 1 REF C32368 UDI-DI code: 15099590720568 Intended Use- For
Beckman Coulter, Inc.

Due to manufacturing issue (incorrectly processing) with in vitro multidrug resistant test.

NHTSA2026-04-144,922 units
Loss of Drive Power due to Transmission Misalignment
Ford Motor Company

Excessive wear of the transmission and transfer case splines may result in a loss of drive power or vehicle rollaway, increasing the risk of a crash.

NHTSA2026-04-144,351 units
Missing Front Axle Hub Spindle Nut
Ford Motor Company

A missing spindle nut may lead to brake system damage or wheel detachment, resulting in a loss of vehicle control and increasing the risk of a crash.

NHTSA2026-04-141,392,935 units
Unexpected Downshift Can Cause Loss of Control
Ford Motor Company

Unexpectedly downshifting into second gear may result in a loss of vehicle control, increasing the risk of a crash.

NHTSA2026-04-1416,994 units
Loss of Rear Brakes
Harley-Davidson Motor Company

Loss of the rear brakes increases the risk of a crash.

NHTSA2026-04-13122 units
Incorrect Seating Capacity on Label/FMVSS 110
Jayco, Inc.

Unbelted passengers may not be properly restrained in a crash, increasing their risk of injury.

NHTSA2026-04-13141,032 units
Fuel Leak at Pipe Connection
Kia America, Inc.

A fuel leak increases the risk of a fire.