Weekly Recall Recap

2026-03-23 to 2026-03-29

64
Recalls
285,483
Units
11
Injuries
1
Deaths

Sources: NHTSA, CPSC, FDA_DRUG, FDA_FOOD, FDA_DEVICE

Other Recalls

NHTSA2026-03-274,476 units
Seat Belts Mail Fail to Properly Restrain Passengers/FMVSS 207, 210
Lucid USA, Inc.

An insufficient weld may prevent the seat belt from properly restraining a passenger, increasing the risk of injury during a crash.

CPSC2026-03-26
AirClub Convertible Bassinets Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violates Mandatory Standard for Bedside Sleepers

The recalled convertible bassinets violate the mandatory standard for bedside sleepers because the mechanism used to attach the product to the adult bed creates an opening between the bedside sleeper and mattress, posing a deadly fall hazard to infants.

CPSC2026-03-26
Nexgrill Recalls Over 10.2 Million Metal Wire Bristle Grill Brushes Due to Ingestion Hazard; Sold at Home Depot

Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that could require surgery.

NHTSA2026-03-261,091 units
TPMS May Not Illuminate for Low Pressure/FMVSS 138
Aston Martin The Americas

Underinflated tires increase the risk of a crash.

CPSC2026-03-26
4our Kiddies Tip Restraint Kits Recalled Due to Tip-Over Hazard; Risk of Serious Injury and Death

The recalled plastic tip restraint kits (also referred to as furniture straps) can break or degrade, posing tip-over and entrapment hazards that can result in serious injuries or death to children or elderly consumers interacting with furniture that is secured to the wall with the defective plastic tip restraints. This is a hidden defect because consumers who purchase and install this product may be under a false sense of security that their furniture is safe from a tip-over incident.

CPSC2026-03-26
CCCEI Brand Power Strips Recalled Due to Risk of Serious Injury or Death from Fire; Sold by Middle Way Electronics

The power strips do not contain supplementary overcurrent protection, which creates a risk of fire if the power strips are overloaded. The resulting fire can cause serious injury or death from smoke inhalation and burns.

CPSC2026-03-26
DIY Cold Plunge Recalls Sauna Heater Kits Due to Risk of Serious Injury or Death from Fire Hazard
Plunge Buddy LLC, doing business as DIY Cold Plunge, of North Mankato, Minnesota

Electrical conductors within the sauna heater kits can overheat, posing a fire hazard and risk of serious injury or death.

CPSC2026-03-26
DuraTrac Recalls Stainless Steel Gas Connectors Due to Fire Hazard

The recalled DuraTrac gas connectors contain a manufacturing defect that could cause a gas leak, posing a fire hazard to consumers.

CPSC2026-03-26
FUNTOK Ride-On Trucks Recalled Due to Fire and Burn Hazards; Risk of Serious Injury or Death; Imported by Shenzhen Luobei Trading

The truck's circuit board can overheat and ignite, posing fire and burn hazards.

CPSC2026-03-26
GLMZZ Fidget Magnet Ball Toys Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys

The magnet ball toys violate the mandatory standard for toys because they are high-powered magnets, posing an ingestion hazard to children. When high-powered magnets are swallowed, they can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.

CPSC2026-03-26
MPINOI 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; Sold on Amazon by Bioenrrty

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.

CPSC2026-03-26
Petzl America Recalls Nomic and Ergonomic Ice Climbing Axes Due to Fall Hazard; Risk of Serious Injury or Death

The ice axe shaft can break at the handle during use, posing a fall hazard, which can result in serious injury or death.

CPSC2026-03-26
Sunnyyes LED Mini Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries

The recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because the lights contain lithium coin batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the screw used on the remote controls to secure the battery compartments that contain a lithium coin battery does not remain attached. Also, the packaging does not have the warnings as required by Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

CPSC2026-03-26
Vive Health Recalls Adult Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Two Deaths Reported

When the recalled bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress. This poses a serious entrapment hazard and risk of death by asphyxiation.

NHTSA2026-03-26105 units
Improperly Sealed Side Curtain Air Bags/FMVSS 226
Chrysler (FCA US, LLC)

Air bags with insufficient pressure retention increase the risk of ejection and injury during a crash.

NHTSA2026-03-26178,246 units
Improperly Sealed Side Curtain Air Bags/FMVSS 226
Chrysler (FCA US, LLC)

Air bags with insufficient pressure retention increase the risk of ejection and injury during a crash.

NHTSA2026-03-266 units
GAWR on Federal Placard May Exceed Tire Load Rating/FMVSS 120
Gillig, LLC

Referencing an incorrect GAWR can lead to unintentionally overloading the rear tires, increasing the risk of a crash.

NHTSA2026-03-2651 units
Park Outside: High Voltage Battery Modules May Short Circuit
Nissan North America, Inc.

A short circuit in a high voltage battery module increases the risk of a fire.

FDA Drug2026-03-25
FDA Recall: Children's Ibuprofen Oral Suspension, USP, 100 mg per 5mL, 4 FL OZ (120 mL) bottle, Manufactured for
STRIDES PHARMA INC

Presence of foreign substance: the firm received complaints for a gel-like mass and black particles in the product.

FDA Food2026-03-25
FDA Recall: Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC
Winder Laboratories, LLC

Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.

FDA Food2026-03-25
FDA Recall: MID EAST Jordanian Zaatar spice mix; NET Wt. 5lb plastic bag; UPC: 094379607038 Packed by: Propack
Kradjian Importing Company, Inc.

Undeclared allergen ingredients (sesame and wheat) in Zaatar Spice mix.

FDA Food2026-03-25
FDA Recall: Butter-Rich Powder, Net Weight 50 LB., packaged in a multiply Kraft bag with poly liner
Bluegrass Ingredients Inc.

Potential Salmonella contamination

FDA Device2026-03-25
FDA Recall: Artegraft Vascular Graft; REF#: AG740;
LeMaitre Vascular, Inc.

Labeling mix-up resulting in the incorrect lot outer packaging of product.

FDA Device2026-03-25
FDA Recall: Convatec, EsteemBody Drainable Pouch REF:423653 10-35mm
ConvaTec, Inc

Drainable large pouch may leak due to manufacturing issue.

FDA Device2026-03-25
FDA Recall: Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1, a device that displays medic
GE Medical Systems, LLC

There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.

FDA Device2026-03-25
FDA Recall: Convatec, EsteemBody Drainable Pouch REF:423643, 10-45mm
ConvaTec, Inc

Drainable large pouch may leak due to manufacturing issue.

FDA Food2026-03-25
FDA Recall: GREENWAY FARMS of Georgia GARLIC DILL PICKLES CHIPS Net Wt 16 fl oz (473 ml) UPC 8 57866 00501 0 Pro
BlueFrog Foods

No process authority

FDA Device2026-03-25
FDA Recall: Cub Pediatric Crib, Model FL19H
Stryker Medical Division of Stryker Corporation

Cribs sold in the USA are missing two access door warning labels.

FDA Drug2026-03-25
FDA Recall: Dexamethasone Sodium Phosphate Injection, USP, 100 mg/ 10 mL, (10 mg/mL), 10x10 mL Multiple Dose Via
SOMERSET THERAPEUTICS LLC

Failed Impurities/Degradation Specifications - OOS impurities result observed during long term stability testing at product expiry (24 months) were above specs for these impurities: Dexamethasone Sodium Phosphate EP impurity G (Impurity RU 49336) and dexamethasone formate.

FDA Food2026-03-25
FDA Recall: Wawa Chocolate Low-fat Milk 16 oz , (Pint) Plastic bottle .Store Refrigerated
Wawa Beverage Company

Foreign plastic material discovered on fill line.

FDA Food2026-03-25
FDA Recall: Simply Nature, Spinach Bites, 12 oz retail unit, Plastic wrapped bites inside of a retail box. Keep
Dr. Praeger's Sensible Foods Inc.

This product has the possibility of contamination with rodent hair.

FDA Device2026-03-25
FDA Recall: Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion Leksell Gamma
Elekta, Inc.

Due to adapter not being properly aligned or locked in place.

FDA Food2026-03-25
FDA Recall: Wawa Cookies & Cream Milk 16 oz (Pint), Plastic bottle Store Refrigerated
Wawa Beverage Company

Foreign plastic material discovered on fill line.

FDA Device2026-03-25
FDA Recall: MICS3 Angled Sagittal Saw Attachment; Part Number: 210490
Howmedica Osteonics Corp.

A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment. These screws, which secure the cover to the Angled Saw Housing, may loosen during use and detach from the attachment.

FDA Food2026-03-25
FDA Recall: TETAS Mireya, Cherry Milkshake (Colita con Leche), i unit Popsicle, Net wt 6OZ. 170GRS. KEEP FROZEN
ASUKAR FOODS CORP

Undeclared allergen: Soy Lecithin

FDA Device2026-03-25
FDA Recall: Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/Catalog Number: 303585 Product
Hologic, Inc.

Due to product exhibiting potential to generate either invalid or false negative results.

FDA Food2026-03-25
FDA Recall: Miss Vickies Spicy Dill Pickle; 8 oz bag
FRITO-LAY NORTH AMERICA, INC.

Undeclared Allergen: Milk

FDA Device2026-03-25
FDA Recall: Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog N
Baxter Healthcare Corporation

Display screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in susceptible individuals.

FDA Device2026-03-25
FDA Recall: Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1, a device that displays medica
GE Medical Systems, LLC

There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.

FDA Device2026-03-25
FDA Recall: Product Name: ID NOW" Influenza A & B 2 Model/Catalog Number: 427-000 Software Version: Not Applic
Abbott Diagnostics Scarborough, Inc.

It was confirmed that the impacted lot has a higher occurrence of invalid rates when compared to the product Instructions for Use.

FDA Food2026-03-25
FDA Recall: Butter Powder, Net Weight 50 LB., packaged in a multiply Kraft bag with poly liner
Bluegrass Ingredients Inc.

Positive Salmonella contamination

FDA Device2026-03-25
FDA Recall: Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 SP7.1, a device that displays m
GE Medical Systems, LLC

There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.

FDA Food2026-03-25
FDA Recall: GREENWAY FARMS of Georgia JALAPENO DILL PICKLES CHIPS Net Wt 16 fl oz (473 ml) UPC 8 57866 00506 5 P
BlueFrog Foods

No process authority

FDA Food2026-03-25
FDA Recall: CLOVER SONOMA COTTAGE CHEESE LOW FAT 2% MILKFAT NET WT 16OZ UPC 0 70852 54400 7 & 32OZ UPC 0 70852
SAPUTO CHEESE USA, INC

Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.

FDA Food2026-03-25
FDA Recall: Great Value Cottage Cheese Small Curd 4% Milkfat NET WT 16oZ UPC 0 78742 37235 8; 24oz UPC 0 78742 3
SAPUTO CHEESE USA, INC

Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.

FDA Food2026-03-25
FDA Recall: Wawa Double Dutch Chocolate Milk ,16 oz (Pint) Plastic bottle Store Refrigerated
Wawa Beverage Company

Foreign plastic material discovered on fill line.

FDA Food2026-03-25
FDA Recall: Great Value Lowfat Cottage Cheese Small Curd 2% Milkfat NET WT 24OZ UPC 0 78742 11673 0 DISTRIBUTED
SAPUTO CHEESE USA, INC

Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.

FDA Food2026-03-25
FDA Recall: Wawa Reduced Fat Milk 2% 16 oz (Pint)
Wawa Beverage Company

Foreign plastic material discovered on fill line.

FDA Drug2026-03-25
FDA Recall: Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 0.2%/0.5%*, 5 mL, Rx Only, Sterile, Apotex
Apotex Corp.

Lack of Assurance of Sterility

NHTSA2026-03-2574 units
Entry Steps May Extend While in Transit
Storyteller Overland

Steps extending while in transit increase the risk of a crash.

NHTSA2026-03-2575,323 units
Instrument Panel Failure/FMVSS 101
Volkswagen Group of America, Inc.

An instrument panel that does not display critical safety information, such as the speedometer or warning lights, can increase the risk of a crash.

FDA Drug2026-03-25
FDA Recall: Webcol Alcohol Prep pad (70% isopropyl alcohol) 2 ply, 200 count boxes, Cardinal Health 200 LLC 3651
Cardinal Health 200, LLC

Microbial Contamination of Sterile Products: Affected lots have been deemed non-sterile following discovery of a contaminant (Paenibacillus phoenicis), which may pose a potential infection risk to vulnerable groups.

FDA Food2026-03-25
FDA Recall: CLOVER SONOMA SOUR CREAM NET WT 8OZ UPC 0 70852 61800 5 & 16OZ UPC 0 70852 61500 4 DISTRIBUTED BY:
SAPUTO CHEESE USA, INC

Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.

FDA Drug2026-03-25
FDA Recall: Pitavastatin Tablets, 2 mg, packaged in 90-count bottles, Rx only, Manufactured for: Northstar Rx LL
Annora Pharma Private Limited

Presence of foreign tablets/capsules: one Pitavastatin tablet 1mg found in bottle of Pitavastatin tablets 2mg

FDA Device2026-03-25
FDA Recall: Convatec, EsteemBody Drainable Pouch REF:423657 10-35mm
ConvaTec, Inc

Drainable large pouch may leak due to manufacturing issue.

FDA Food2026-03-25
FDA Recall: Great Value Fat Free Cottage Cheese Small Curd 0% Milkfat NET WT 24OZ UPC 0 78742 37339 3 DISTRIBU
SAPUTO CHEESE USA, INC

Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.

FDA Device2026-03-25
FDA Recall: Brand Name: STA Liatest D-Di Product Name: STA Liatest D-Di Model/Catalog Number: REF 00515 Produ
Diagnostica Stago, Inc.

After receiving customer complaints, investigations confirmed the presence of a positive bias in D-Dimer measurements throughout the entire analytical range.

FDA Food2026-03-25
FDA Recall: Dreamland's Zaatar Chickpea Salad is packaged in poly bags with a generic label which declares "chic
Dreamland Inc

Undeclared Sesame, Soy, Wheat

FDA Device2026-03-25
FDA Recall: Battery Charging Station; Model: 0998-00-0802;
Datascope Corp.

The Battery Charging Station is an optional dual-bay charger used to charge the Cardiosave IABP Lithium- Ion batteries when they are not being used to operate the IABP. Getinge has identified that a protruding screw in the left battery bay limits full insertion of certain batteries and prevents proper charging. The right bay of the Battery Charging Station is not affected by this issue.

NHTSA2026-03-241,446 units
Inadequate Turn Signal Luminosity/FMVSS 108
Winnebago Industries, Inc.

A small lens can make it difficult for other drivers to see the turn signal, increasing the risk of a crash.

NHTSA2026-03-2444 units
Incorrect Information on Tire Placard/FMVSS 110
Bentley Motors, Inc.

Incorrect tire information can allow an incorrectly sized tire to be installed or result in improperly inflated tires, increasing the risk of a crash.

NHTSA2026-03-248,230 units
Incorrect Load Carrying Capacity on Label/FMVSS 110
Toyota Motor Engineering & Manufacturing

A vehicle with an incorrect maximum capacity weight value may be overloaded, which can increase the risk of a crash.

NHTSA2026-03-2415,264 units
Front Passenger Air Bag May Not Deploy Properly/FMVSS 208
Toyota Motor Engineering & Manufacturing

Incorrect detection of an occupant may result in improper air bag deployment during a crash, increasing the risk of injury.

NHTSA2026-03-231,127 units
Entry Steps May Extend While in Transit
Grand Design RV, LLC

Steps extending while in transit increase the risk of a crash.