Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

751–775 of 26077

HighCPSC·26466·2026-05-07
Battery-operated Light Up Toys Recalled for Risk of Battery Ingestion
ZMC Group is recalling about 124,560 battery-operated light-up toys because they contain easily accessible button cell batteries that can cause serious internal injuries or death if swallowed by children. Consumers should stop using the toys immediately and contact the manufacturer for a refund.
Product
Various Battery-operated Light Up Toys
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26470·2026-05-07
Multi-Purpose Helmets Recalled for Serious Head Injury Risk
Multi-purpose helmets sold on Temu by Foubeaka and Geniuss are recalled because they violate mandatory bicycle helmet safety standards and can fail to protect users in a crash, posing a serious risk of injury or death.
Product
Multi-Purpose Helmets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26472·2026-05-07
Justforjoyful Rainbow Wall Toys Recalled for Choking Hazard Risk
The CPSC has recalled Justforjoyful Rainbow Wall Toys because the drumstick attached to the xylophone component has a spherical end that violates the mandatory children's toy safety standard and poses a choking hazard. About 160 units were sold on Amazon from December 2025 through March 2026.
Product
Justforjoyful Rainbow Wall Toys
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26467·2026-05-07
Favoto Model H-1 Bicycle Helmets Recalled for Serious Head Injury Risk
Favoto Model H-1 bike helmets violate mandatory safety standards and may fail to protect users in a crash, posing a risk of serious head injury or death. About 2,200 units sold on Amazon from April 2022 through January 2026 are affected.
Product
Favoto Bike Helmets
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·25V474000·2026-05-07
Genesis G90 and GV60 vehicles recalled for instrument panel display software error
Hyundai is recalling 2023-2025 Genesis G90 and GV60 vehicles for a software error that causes instrument panel display failures. A failed display hides critical safety info like the speedometer and warning lights, increasing crash risk.
Product
GENESIS — 2024 GENESIS G90
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V471000·2026-05-07
2024-2025 Chrysler Pacifica rearview camera display failure recall
Chrysler recalled 2024-2025 Pacifica vehicles for faulty radios preventing rearview camera display, which reduced rear visibility and increased crash risk. Dealers replaced the radios free of charge, and all affected vehicles have been repaired.
Product
CHRYSLER — 2025 CHRYSLER PACIFICA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V473000·2026-05-07
2025-2026 Grand Design Lineage recreational trailers recalled for door latch failure
Grand Design is recalling 2025-2026 Lineage recreational trailers with Lippert Modularia entrance doors. The door latch mechanism may fail, preventing occupants from exiting during an emergency.
Product
GRAND DESIGN — 2025 GRAND DESIGN LINEAGE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·26478·2026-05-07
EVLWZL and Gunugu Mattresses Recalled for Fire Hazard Risk
EVLWZL and Gunugu mattresses violate mandatory flammability standards and pose a risk of serious injury or death from fire. Approximately 670 units sold through Amazon, Walmart, and Wayfair from October 2025 through March 2026 are affected.
Product
EVLWZL and Gunugu Mattresses
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2031-2026·2026-05-06
Insulin Pump Batteries Recalled After Sudden-Shutdown Reports
OmniDose is recalling 23,000 lithium battery packs used in its X4 insulin pumps after reports of unexpected shutdown.
Product
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: GENERAL KIT, Medline Kit Number/SKU DYNJ905664I
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1984-2026·2026-05-06
Immy Myco DDR Trident Neutralization Buffer B Recalled for Potential Contamination
Immuno-Mycologics, Inc. is recalling Immy Myco DDR Trident Bulk Neutralization Buffer B (60 X 30 mL, Lot F5061154) because the product may contain contaminants. The buffer is used for clinical specimen processing for Mycobacterium spp. diagnosis.
Product
Immy, Myco DDR Trident, Bulk Neutralization Buffer B (60 X 30 mL), REF: TBPN67-60 For processing of clinical specimens for Mycobacterium spp. diagnosis
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0492-2026·2026-05-06
GenTeal Tears Lubricant Eye Gel Recalled Due to Sterility Concerns
Alcon Research LLC is recalling GenTeal Tears Lubricant Eye Gel nationwide due to FDA inspection observations indicating the product may lack assurance of sterility. Consumers should not use affected lots.
Product
GENTEAL TEARS — GENTEAL TEARS (HYPROMELLOSE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1947-2026·2026-05-06
AIDBAG First Aid Kits with Recalled Blood Glucose Meters Recalled
North American Rescue LLC. is recalling AIDBAG first aid kits containing McKesson TRUE Metrix PRO blood glucose meters that display an E-5 error code incorrectly, potentially delaying appropriate patient treatment.
Product
AIDBAGs are first aid kits of convenience composed of individually labeled devices designed as specialty first aid kits designed for the appropriate level provider to evaluate and treat patients at the point-of-injury / point-of-illness. The original manufacturer labeling, includ
Category
Medical Device
Distribution
2 states
SevereFDA (Devices)·Z-2021-2026·2026-05-06
Medline and Centurion Medical Procedure Kits Recalled for High Endotoxin Levels
Medline Industries is recalling Medline and Centurion medical procedure kits containing neuro sponges due to higher-than-expected endotoxin levels that may cause the products to be out-of-specification.
Product
Medline and Centurion medical procedure kits, containing Medline Neuro Sponges (1229 in total), HEAD & NECK TRAY, SINUS, SMR, etc.
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1771-2026·2026-05-06
Boston Scientific Cardiac Pacemakers Require Software Update
Boston Scientific is expanding a software advisory for ACCOLADE family pacemakers and cardiac resynchronization therapy devices. Updated software (Brady SMR6) is now available to address identified issues.
Product
Boston Scientific Cardiac Resynchronization Therapy (CRT)labeled as: 1. VALITUDE CRT-P EL, Model Number U125; 2. VALITUDE CRT-P EL MRI, Model Number U128; 3. VISIONIST CRT-P EL, Model Number U225; 4. VISIONIST CRT-P EL, Model Number U226; 5. VISIONIST CRT-P EL MRI, Mod
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-2016-2026·2026-05-06
Medline Medical Procedure Kits with Neuro Sponges Recalled
Medline is recalling multiple medical procedure kits containing Neuro Sponges due to higher-than-expected endotoxin levels that may render the product out-of-specification.
Product
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. OPEN HEART CDS PART A, Medline Kit Number/SKU CDS840402AI; 2. OPEN HEART CDS, Medline Kit Number/SKU CDS984890V; 3. RR-NEURO VASCULAR PACK-LF, Medline Kit Number/SKU DYNJ0394874L; 4.
Category
Medical Device
Distribution
0 states
SevereFDA (Drugs)·D-0491-2026·2026-05-06
Systane Lubricant Eye Gel Recalled Due to Sterility Concerns
Alcon Research LLC is recalling Systane Lubricant Eye Gel Night Gel (10g) distributed nationwide due to FDA inspection observations regarding lack of assurance of sterility that may impact product quality.
Product
SYSTANE — SYSTANE (HYPROMELLOSE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0499-2026·2026-05-06
Optase Dry Eye Drops Recalled for Lack of Sterility Assurance
Scope Health is recalling Optase Dry Eye Intense Drops (Glycerin 0.2%) due to lack of assurance of sterility. The product is distributed nationwide.
Product
OPTASE — OPTASE (GLYCERIN)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1827-2026·2026-05-06
WHILL Model F Powered Wheelchair Bluetooth Communication Vulnerability
WHILL, INC. is recalling WHILL Model F powered wheelchairs with software versions before HMI 2.23 and MC 1.05 due to a Bluetooth Low Energy (BLE) communication vulnerability identified through the CISA Vulnerability Disclosure Program.
Product
WHILL Model F, with software versions before HMI: 2.23 / MC: 1.05; the device is an indoor/outdoor, foldable battery-operated 2-wheel drive (rear-wheel drive) powered wheelchair.
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1770-2026·2026-05-06
Boston Scientific Pacemakers Subject to Software Update Advisory
Boston Scientific is issuing a software update (Brady SMR6) for certain ACCOLADE and PROPONENT pacemakers and cardiac resynchronization therapy devices. The advisory population is expanding to include all dual-chamber extended life and CRT-P devices.
Product
Boston Scientific Pacemaker, Implantable Pulse Generator, Pacemaker (non- Cardiac Re-Synchronization Therapy) labeled as: 1. ESSENTIO SR SL, Model Number L100; 2. ESSENTIO DR SL Pacemaker, Model Number L101; 3. ESSENTIO SR SL MRI Pacemaker, Model Number L110; 4. ESSENTIO
Category
Medical Device
Distribution
0 states
SevereFDA (Food)·H-0686-2026·2026-05-06
Korean Enoki Mushroom Recall Due to Listeria Monocytogenes Contamination
Black-label enoki mushroom, lot 215, tested positive for Listeria monocytogenes. The product was distributed to accounts in California, Florida, and Maryland.
Product
Black label with blue lettering. FOOD Korean Food, ENOKI MUSHROOM, 150g clear plastic package; Product of Korea, Keep Refrigerated. Distributed by Hemu Trading Inc. UPC: 8801234567893
Category
Food
Distribution
3 states
SevereFDA (Devices)·Z-1996-2026·2026-05-06
iLet Bionic Pancreas Software Versions Recalled for Delayed CGM Readings
Beta Bionics is recalling iLet Bionic Pancreas units with software versions 1.4.2 and 1.4.3 due to a compatibility issue with Dexcom G7 sensors that can cause delayed glucose readings and loss of automatic insulin adjustments.
Product
iLet Bionic Pancreas, REF: BB1001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2030-2026·2026-05-06
Medline Microdisectomy Kits Recalled for High Endotoxin Levels
Medline is recalling Microdisectomy Packs containing Neuro Sponges due to higher-than-expected endotoxin levels found during an internal review. The affected products may be out-of-specification for endotoxin.
Product
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. MICRODISECTOMY PACK, Medline Kit Number/SKU DYNJ80585B; 2. MICRODISECTOMY PACK, Medline Kit Number/SKU DYNJ80585C; 3, MICRODISECTOMY PACK, Medline Kit Number/SKU DYNJ80585D.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2013-2026·2026-05-06
Medline Medical Procedure Kits with Neuro Sponges Recalled
Medline Industries is recalling medical procedure kits containing Neuro Sponges due to higher-than-expected endotoxin levels that may be out of specification. The kits were distributed worldwide.
Product
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. NEURO PACK, Medline kit number/SKU DYNJ64479; 2. CRANIO/NEURO/SPINE, Medline kit number/SKU DYNJ901072D.
Category
Medical Device
Distribution
0 states
HighFDA (Food)·H-0677-2026·2026-05-06
52USA Brand Popping Boba Recalled for Unapproved Food Colorings
52USA brand popping boba in passion fruit flavor is being recalled because the product contains unapproved food colorings including tartrazine and sunset yellow. Approximately 5,196 units were distributed in New York.
Product
52USA brand POPPING BOBA; PASSION FRUIT FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fructose syrup, food additives (hydroxypropyl distarch phosphate (E1442), calcium lactate (E327), DL-malic acid (E296), sodium alginate (E401), citric acid (E330), carrageenan (EE407
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-1943-2026·2026-05-06
Mesh Style Tip Protectors recalled lacking FDA clearance
Healthmark Industries Co., Inc. is recalling Mesh Style Tip Protectors (models CSW-03-2.0 and CSW-04-4.0) distributed nationwide because the product does not have FDA clearance.
Product
Mesh Style Tip Protectors CSW-03-2.0 Open-end style CSW-04-4.0 Closed-end style
Category
Medical Device
Distribution
Distributed nationwide

Filters

751–775 of 26077