Weekly Recall Recap

NewerOlder

2026-07-13 to 2026-07-19

82
Recalls
1,343,501
Units
4
Injuries
0
Deaths

Sources: NHTSA, CPSC, FDA_FOOD, FDA_DRUG, FDA_DEVICE

Other Recalls

NHTSA2026-07-17309 units
Turntable Fasteners Not Heat Treated
Altec Industries, Inc.

A fastener that has not been heat treated could fail, resulting in separation of the pedestal and turntable, increasing the risk of injury.

NHTSA2026-07-1715,628 units
Battery Cable May Short Circuit
International Motors, LLC

A short circuit increases the risk of a fire.

NHTSA2026-07-1750 units
Body Panel Joints Incorrectly Attached/FMVSS 221
International Motors, LLC

The body panels may separate during a crash, reducing structural integrity and increasing the risk of injury.

NHTSA2026-07-1722,730 units
Body Panel Joints Incorrectly Attached/FMVSS 221
International Motors, LLC

The body panels may separate during a crash, reducing structural integrity and increasing the risk of injury.

CPSC2026-07-16116,908 units
TOMY Recalls Boon PIVOT Collapsible Toddler Tower Kitchen Step Stools Due to Risk of Serious Injury and Death from Tip-Over and Fall Hazards
TOMY International, Inc., of Oak Brook, Illinois

The recalled toddler towers can tip over while in use, posing a risk of serious injury and death, due to tip over and fall hazards.

CPSC2026-07-165,952 units
SDADI Kitchen Step Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by Yiwushi Bihe Trading
Yiwushi Bihe Trading Co., Ltd., of China

The recalled tower stools can collapse or tip over while in use, and a child's torso can fit through the openings on the front and back sides, posing a risk of serious injury and death due to tip over, fall and entrapment hazards.

CPSC2026-07-1611,480 units
Panasonic Recalls Electric Toaster Ovens Due to Shock and Fire Hazards
Panasonic Manufacturing (Xiamen) Co., Ltd, of Xiamen, Fujian, China

The power cord insulation can be insufficient due to a protective fiberglass sleeve not covering it adequately, posing a risk of shock and/or fire hazard.

CPSC2026-07-161,012 units
Oitnlaughter Projecting Finger Light Toys Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by Delightmi
Shenzhen Dami Trading Co., Ltd., dba Delightmi, of China

The recalled finger lights violate the mandatory safety standard for toys because they contain 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.

CPSC2026-07-165,900 units
Madewell Recalls Women's Sweaters Due to Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Clothing Textiles
J. Crew Group, LLC of New York, New York

The recalled sweaters violate the mandatory standard for clothing textiles, posing a risk of serious burn injuries or death.

CPSC2026-07-164,200 units
Liizousuda Paint Thinner Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging; Sold on Amazon.com by Shenzhen Gudebo Technology
Shenzhen Gudebo Technology Co. Ltd., of China

The paint thinner contains low-viscosity petroleum distillates, which must be in child-resistant packaging, as required by the?Poison Prevention Packaging Act. The bottles are not child-resistant, posing a risk of serious injury or death from poisoning if the contents are swallowed by young children. Additionally, petroleum distillates can get into the lungs, causing chemical pneumonia and/or pulmonary damage, which can be fatal.

CPSC2026-07-1613,200 units
Jobon Torch Lighters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violate Mandatory Standard for Multipurpose Lighters
Madewell Inc., of Wenzhou Zhongbang Smoking Set Manufacturing Co., Ltd., doing business as Jobon Official Store, of China

The lighters violate the mandatory safety standard for multipurpose lighters because they do not have the required child-resistant mechanisms posing a risk of serious injury or death from fire and burn hazards. In addition, the lighters failed to meet the pre-market lighter submission requirement needed to demonstrate that the lighters feature child-resistant mechanisms and ensuring their safety and compliance with U.S. regulations.

CPSC2026-07-16180 units
Wade Logan Annyka 9-Drawer Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Imported by Ningbo Jiangdong Peter International Trading
Wuxi Leclaire Home Products Co., Ltd., of China

The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory safety standard as required by the STURDY Act.

CPSC2026-07-16211,000 units
Target Recalls Cat & Jack Children's Sandals Due to Risk of Serious Injury or Death from Choking Hazard
Target, of Minneapolis, Minnesota

The sandals' decorative pearls can fall off, posing a risk of serious injury or death from a choking hazard.

CPSC2026-07-16504 units
Noerishia 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 Hurzein
Dongguan Shinneng Huizheng Network Technology Co., Ltd., dba Hurzein

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.

CPSC2026-07-16330 units
MNIENT Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails
Zhuzhoushizuisuanshangmaoyouxiangongsi, 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. The bed rails do not meet structural stability or retention strap requirements, posing a fall hazard. Additionally, the bed rails' push pins and push pin holes are incorrectly sized, posing a laceration hazard.

CPSC2026-07-167,200 units
Huish Outdoors Recalls Hollis Diving Regulators Due to Risk of Serious Injury or Death from Drowning
Huish Outdoors, LLC, of Salt Lake City, Utah

The regulator inlet tube can crack and break, posing a risk of serious injury or death from drowning.

CPSC2026-07-16447 units
Currey & Company Recalls Nottaway Chandeliers Due to Risk of Serious Injury or Death from Electrocution Hazard
Currey & Company, of Atlanta, Georgia

The recalled chandeliers lack proper electrical grounding, posing a risk of serious injury or death from electrocution hazard.

NHTSA2026-07-16641 units
Steel Wheels May Crack and Separate
Chrysler (FCA US, LLC)

Loss of vehicle control increases the risk of a crash.

NHTSA2026-07-1615,535 units
Water May Damage Rearview Camera
Jaguar Land Rover North America, LLC

A rearview camera image that does not display can decrease the driver's visibility, increasing the risk of a crash.

NHTSA2026-07-16168,149 units
Incorrect GAWR on Certification Label/FMVSS 110
Nissan North America, Inc.

An overloaded vehicle can increase the risk of a crash.

NHTSA2026-07-16884 units
Unprotected Boom Stow Wire May Short and Cause Fire
Altec Industries, Inc.

An overheated wire can ignite flammable material in the cargo area, increasing the risk of fire.

CPSC2026-07-167,000 units
Warren James Recalls the Copper Cup Found in Flashgitz Relic Lunch Boxes Due to Risk of Serious Injury or Death from Lead Poisoning
Warren James, Inc., of Santa Monica, California

The cup in the lunch boxes contains high lead concentration levels for drinking vessels, posing a lead poisoning hazard. Lead is toxic if ingested by adults or children and can cause adverse health issues.

NHTSA2026-07-15387,911 units
Second-Row Seat May Move Unexpectedly
Ford Motor Company

A seat that moves unexpectedly may not properly restrain an occupant during a crash, increasing the risk of injury.

NHTSA2026-07-1524 units
Frame Rails May Crack
Orange EV

A detached rail can cause a loss of control, increasing the risk of injury.

NHTSA2026-07-1547,749 units
Seat Belt Buckle May Fail
Hyundai Motor America

A seat belt buckle that fails to properly restrain an occupant in a crash increases the risk of injury.

NHTSA2026-07-15159 units
Drive Mode May Disengage Causing a Loss of Drive Power
E-One Incorporated

Loss of power to the rear wheels can prevent the vehicle from moving, increasing the risk of a crash.

NHTSA2026-07-15134 units
Printed Circuit Board May Overheat
Winnebago Industries, Inc.

An overheated printed circuit board increases the risk of a fire.

FDA Food2026-07-15
FDA Recall: Bakr Brown Butter Chocolate Chunk Ready to Bake Cookie Dough, 8-oz pouch 12 cookies per pouch, UPC 8
Bear Stewart Co

undeclared soy

FDA Food2026-07-15
FDA Recall: EC Hot Links Seasoning 45.05#
Adams Extract & Spice LLC

Undeclared Sesame allergen

FDA Food2026-07-15
FDA Recall: Wise Onion Rings, 3.75 oz, metalized film in cardboard cartons, 14 bags per case,
Wise Foods Inc

The product contains undeclared Yellow 5 and 6, Blue 1, and unapproved Red 3.

FDA Food2026-07-15
FDA Recall: Trafa Pharmaceuticals Inc. brand ORGANIC MORINGA LEAF POWDER; NET WEIGHT: 15 KGS; packaged in brown
Trafa Pharmaceutical Inc.

Potential contamination with Salmonella

FDA Food2026-07-15
FDA Recall: Vanilla Dessert Shells (Giant), 6 dessert shells/1 package, 1 dessert shell is approximately 23.67 g
Specialty Bakers, LLC

Undeclared Allergen (Soy)

FDA Food2026-07-15
FDA Recall: Coopers Bbq 60 Gal Bean Mix box
Adams Extract & Spice LLC

Undeclared Sesame allergen

FDA Food2026-07-15
FDA Recall: Alabama Banana Pudding Marshmallow, 4 ounce 16 pieces of individual marshmallows packaged in a seale
Wondermade LLC

Foreign material: small metal pieces

NHTSA2026-07-15315 units
Trailer Brakes and Lighting May Be Lost/FMVSS 108
Ford Motor Company

A loss of trailer brakes or lights can reduce the driver’s ability to control the trailer and decrease the trailers visibility to other road users, increasing the risk of a crash.

NHTSA2026-07-154 units
Liftgate Deck Pins May Break
Wabash National Corporation

A liftgate that falls unexpectedly increases the risk of injury.

FDA Drug2026-07-15
FDA Recall: Gasco Isopropyl Alcohol 70%, Net Contents: 1 US Gallon (3.78 L), Manufactured by: Gasco Industrial C
Gasco Industrial Corp.

Subpotent drug

FDA Drug2026-07-15
FDA Recall: Clomiphene Citrate USP Active Pharmaceutical Ingredient (CAS : 50-41-9), Net Weight a)1 KG (NDC 8484
Shimoga Chemicals

cGMP deviations

FDA Drug2026-07-15
FDA Recall: Pemetrexed for Injection 500mg/Vial, 1 50 mL Single-Dose Vial per carton, For intravenous use only,
Reliance Life Sciences Private Limited

Lack of Sterility Assurance

FDA Drug2026-07-15
FDA Recall: Gasco Isopropyl Alcohol 70%, Net Contents: 16 Oz. (474 mL). Manufactured by: Gasco Industrial Corp.,
Gasco Industrial Corp.

Subpotent drug

FDA Drug2026-07-15
FDA Recall: Drogueria San Juan Puerto Rico Isopropyl Alcohol 70%, 1 gallon (3.78 liter), Distributed by: Droguer
Gasco Industrial Corp.

Subpotent drug

FDA Drug2026-07-15
FDA Recall: Bortezomib for Injection 3.5mg/Vial, 10 mL per Single-Dose Vial, For Intravenous or Subcutaneous Use
Reliance Life Sciences Private Limited

Lack of Sterility Assurance

FDA Drug2026-07-15
FDA Recall: Pemetrexed for Injection 100mg/Vial, 1 10 mL Single-Dose Vial per carton, For intravenous use only,
Reliance Life Sciences Private Limited

Lack of Sterility Assurance

FDA Device2026-07-15
FDA Recall: 5008X Blood Tubing Set, 24 units per case. Includes the below model numbers and descriptions. 1.
Fresenius Medical Care Holdings, Inc.

Potential for Online Port Errors due to connection issues when connecting the SafeLine of the 5008X CAREset to the substitution fluid port of the 5008X CAREsystem.

FDA Drug2026-07-15
FDA Recall: Azacitidine for Injection 100mg/Vial, 1 10 mL Single-Dose Vial per carton, For Subcutaneous and Int
Reliance Life Sciences Private Limited

Lack of Sterility Assurance

FDA Drug2026-07-15
FDA Recall: Drogueria San Juan Puerto Rico Isopropyl Alcohol 70%, 16 oz, 474 mL, Distributed by: Drogueria San J
Gasco Industrial Corp.

Subpotent drug

FDA Drug2026-07-15
FDA Recall: Methohexital Sodium, 100 mg/10 mL (10 mg/mL), Total Volume: 10 mL, Rx only, Compounded drug, QuVa Ph
QuVa Pharma, Inc.

Failed Impurities/Degradation Specifications

FDA Food2026-07-15
FDA Recall: High Valley Orchard Chocolate Covered Raisins, net wt. 15oz. per package, each case contains 12/15oz
Lehi Valley Trading Company, Inc

Undeclared Peanut. High Valley Orchard Chocolate Covered Raisins contains unintended undeclared peanut due to mis-packaging.

FDA Device2026-07-15
FDA Recall: Aquacel Ag Surgical SP REF: 413556 9cm x 15cm/3.5 in. x 6 in., Sterile R
ConvaTec, Inc

Surgical dressing manufactured out of specification (greater thickness).

FDA Device2026-07-15
FDA Recall: GSP Neonatal GALT Kit. Product Codes: 3303-001U, 3303-0010. in vitro diagnostic. Used in FLUORE
WALLAC OY

Reduction in the on-board stability of the GSP GALT assay. This may increase the likelihood of run-QC failures and consequently delay the reporting of patient results.

FDA Device2026-07-15
FDA Recall: Brand Name: Versius Surgical System US Product Name: Vesius Surgeon Console US Model/Catalog Numbe
CMR SURGICAL LIMITED

Secure Boot was mistakenly not enabled at manufacturing time, which presents a potential cybersecurity risk.

FDA Device2026-07-15
FDA Recall: Atellica CH Enzymatic Hemoglobin A1c (A1c_E). Material Number: 11097536.
Siemens Healthcare Diagnostics, Inc.

The potential for intermittent well-to-well bias on the A1c_E assay on the Atellica CH and Atellica CI analyzer which could cause falsely depressed or falsely elevated HbA1c patient results.

FDA Device2026-07-15
FDA Recall: VITEK 2 AST-N447 TEST KIT Product reference 424620
Biomerieux Inc

Potential for false resistant carbapenem and/or cephalosporin results when analyzing samples with kits from affected lot that have pouch foil fractures.

FDA Device2026-07-15
FDA Recall: Intracept Access Instruments, Description/REF: INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035, INTRAC
Boston Scientific Neuromodulation Corporation

Intraosseous nerve ablation system instruments may have sterile barrier breach of the outer tray seal, which may introduce a risk of sterility breach, and if breached could lead to severe infection.

FDA Device2026-07-15
FDA Recall: Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569D; 2) ACCESSORY KIT, Mo
Medline Industries, LP

Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general purpose temperature probe-size 9 due to an error in its distribution control process.

FDA Device2026-07-15
FDA Recall: OmniTract Surgical Retractor System, which includes 633 of the firm s product codes.
Integra LifeSciences Corp. (NeuroSciences)

The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes. Integra LifeSciences has identified that the dry time needs to be extended to 90 minutes, 110 minutes, or 120 minutes depending on the sterilization cycle exposure time used.

FDA Food2026-07-15
FDA Recall: Fresh to You Burger Chicken Fillet, SKU 10150, Net wt. 5oz. Product is refrigerated. UPC 1 00000 010
Fresh & Ready Foods LLC

Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Fillet sandwich. Raw breaded chicken patties pose a risk of foodborne illness due to the potential presence of Salmonella.

FDA Drug2026-07-15
FDA Recall: Drogueria San Juan Puerto Rico Isopropyl Alcohol 70%, 32 oz., 946 mL, Distributed by: Drogueria San
Gasco Industrial Corp.

Subpotent drug

FDA Device2026-07-15
FDA Recall: KL Owen Custom Orthodontic Solution, model/catalog number CIAS-800033,
Klowen Braces

A product error defect may cause incorrect bracket placement.

FDA Device2026-07-15
FDA Recall: Olympus Single Use Distal Cover, Catalog Number MAJ-2315, Used with: EVIS EXERA III Duodenovideoscop
Olympus Corporation of the Americas

Olympus has developed and released newly designed version of the Distal Cover (MAJ-2315) to replace previous design of the Single Use Distal Covers.

FDA Food2026-07-15
FDA Recall: Fresh to You Burger Chicken Fillet Deluxe with Bacon, SKU 10303, Net wt. 5.9oz. Product is refrigera
Fresh & Ready Foods LLC

Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Deluxe With Bacon sandwich. Raw breaded chicken patties pose a risk of foodborne illness due to the potential presence of Salmonella.

FDA Drug2026-07-15
FDA Recall: Methohexital Sodium for Injection, USP 500 mg Multiple Dose Vial, Rx Only, Manufactured by: OneSourc
ONESOURCE SPECIALTY PHARMA LIMITED

Failed Impurities/Degradation Specifications

FDA Device2026-07-15
FDA Recall: MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896
Medtronic MiniMed, Inc.

A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and displays two error messages back-to-back: Pump Error 53 followed immediately by Pump Error 23. Insulin delivery will stop which may lead to delayed therapy and an increased risk of hyperglycemia or diabetic ketoacidosis (DKA).

FDA Food2026-07-15
FDA Recall: Johnny's Salad and Pasta Elegance 5.5 oz (UPC: 0-70381-10014-9) " Johnny's Salad and Pasta Elegance
Adams Extract & Spice LLC

Undeclared Sesame allergen

FDA Drug2026-07-15
FDA Recall: Gasco Isopropyl Alcohol 70%, 32 oz (946 mL) Gasco Industrial Corp., PO Box 1360, Gurabo PR 00778, UP
Gasco Industrial Corp.

Subpotent drug

FDA Food2026-07-15
FDA Recall: Smoked Sausage Spice 32.86#
Adams Extract & Spice LLC

Undeclared Sesame allergen

FDA Device2026-07-15
FDA Recall: Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF, Model Number: DYNJAP10125A
Medline Industries, LP

Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general purpose temperature probe-size 9 due to an error in its distribution control process.

FDA Food2026-07-15
FDA Recall: JB Chicken Sknls 35.73#
Adams Extract & Spice LLC

Undeclared Sesame allergen

FDA Device2026-07-15
FDA Recall: Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 341-
Encore Medical, LP

Due to packaging discrepancy with incorrect product size mixed up.

FDA Device2026-07-15
FDA Recall: Brand Name: Brachytherapy Applicator Product Name: Advanced Gynecological Applicator Product Descr
Elekta, Inc.

Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.

FDA Drug2026-07-15
FDA Recall: Medline Remedy Specialized Silicone Cream (Hydraguard-D ),Manufactured for Medline Industries, LP, T
BioMed Laboratories, LLC.

Failed Impurities/Degradation Specifications; Formaldehyde levels exceeded specification.

FDA Device2026-07-15
FDA Recall: Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote Afterloading
Elekta, Inc.

Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.

FDA Device2026-07-15
FDA Recall: Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569; 2) OPEN HEART PEDS PA
Medline Industries, LP

Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general purpose temperature probe-size 9 due to an error in its distribution control process.

FDA Device2026-07-15
FDA Recall: Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 342-
Encore Medical, LP

Due to packaging discrepancy with incorrect product size mixed up.

FDA Device2026-07-15
FDA Recall: Brand Name: Geneva Product Name: Brachytherapy Applicator Product Description: The device is inten
Elekta, Inc.

Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.

FDA Device2026-07-15
FDA Recall: TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 10
Think Surgical, Inc.

Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array.

NHTSA2026-07-14288,314 units
Roof Rail Covers May Detach
Ford Motor Company

A detached roof rail cover can create a road hazard, increasing the risk of a crash.

NHTSA2026-07-14448 units
Printed Circuit Board May Overheat
Grand Design RV, LLC

An overheated printed circuit board increases the risk of a fire.

NHTSA2026-07-145,290 units
Loss of Steering
Tenneco Automotive

A loss of steering increases the risk of a crash.

NHTSA2026-07-13105 units
ADS Software May Fail to Detect and Respond to Heavy Smoke
Zoox, Inc.

Failing to respond to low visibility conditions can increase the risk of a crash or impede first responders.

NHTSA2026-07-1315 units
Noncompliant Vehicles Incorrectly Imported/FMVSS 208, 201
Tesla, Inc.

A noncompliant vehicle may have reduced occupant protections, increasing the risk of injury during a crash.

NHTSA2026-07-133,794 units
Loss of Steering Control from Loose Steering Arm Fasteners
Volvo Trucks North America

A loose steering arm can result in a loss of vehicle steering control, increasing the risk of a crash.