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

826–850 of 30631

HighNHTSA·25V707000·2026-05-10
[pending] 2025 FOREST RIVER STEALTH EVO
Pending LLM rewrite. Source: NHTSA 25V707000.
Product
FOREST RIVER — 2025 FOREST RIVER STEALTH EVO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V710000·2026-05-10
[pending] 2023 JEEP WRANGLER 4XE
Pending LLM rewrite. Source: NHTSA 25V710000.
Product
JEEP — 2023 JEEP WRANGLER 4XE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V712000·2026-05-10
[pending] 2025 MERCEDES-BENZ SPRINTER 2500
Pending LLM rewrite. Source: NHTSA 25V712000.
Product
MERCEDES-BENZ — 2025 MERCEDES-BENZ SPRINTER 2500
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V616000·2026-05-09
2025 BMW X1 and related vehicles seat belt retractor defect
BMW is recalling certain 2025–2026 BMW X1 and X2 vehicles, along with MINI Cooper and Countryman models, because the front seat belt retractors may be damaged and fail to properly restrain occupants during a crash.
Product
BMW — 2025 BMW X1
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-05092026-01·2026-05-09
DAISY BRAND Headcheese Deli Meat May Contain Listeria
USDA FSIS issued a public health alert for DAISY BRAND headcheese products that may be contaminated with Listeria monocytogenes. The fully cooked deli meat products with a use-by date of March 26, 2026 were distributed to retail delis in Illinois and Indiana.
Product
Crawford Sausage Co., Inc. — FSIS Issues Public Health Alert for Headcheese Deli Meat Products That May Be Contaminated With Listeria
Category
Food
Distribution
2 states
CriticalCPSC·26465·2026-05-07
EEMB Lithium Battery Packs Recalled for Unsafe Child-Resistant Packaging
EEMB lithium coin battery packs sold online are not in child-resistant packaging as required by law. If swallowed by a child, these batteries can cause serious internal injuries or death.
Product
EEMB Lithium Battery Packs
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26475·2026-05-07
Analemma Water Bottles recalled for laceration and ingestion hazards
Analemma Water Bottles are recalled because the inner glass liner can break, posing risk of serious injury or death from laceration and ingestion. The importer has received 20 reports of the glass breaking, including one oral injury.
Product
Analemma Water Bottles
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26477·2026-05-07
Youth Sweatshirts with Drawstrings Recalled for Strangulation Hazard
Allura Imports is recalling about 120 youth sweatshirts with drawstrings due to risk of strangulation. The drawstrings can catch on objects and cause serious injury or death to children.
Product
Youth Sweatshirts with Drawstrings
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26468·2026-05-07
Svnntaa Bed Rails Recalled Due to Entrapment and Asphyxiation Risk
Svnntaa bed rails sold on Amazon violate safety standards and pose a risk of entrapment, asphyxiation, falls, and laceration. Consumers should stop using them immediately and contact Eokeanon for a refund.
Product
Svnntaa Bed Rails
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·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·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
[pending] 2024 GENESIS G90
Pending LLM rewrite. Source: NHTSA 25V474000.
Product
GENESIS — 2024 GENESIS G90
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V472000·2026-05-07
[pending] 2023 JEEP GRAND CHEROKEE
Pending LLM rewrite. Source: NHTSA 25V472000.
Product
JEEP — 2023 JEEP GRAND CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V471000·2026-05-07
[pending] 2025 CHRYSLER PACIFICA
Pending LLM rewrite. Source: NHTSA 25V471000.
Product
CHRYSLER — 2025 CHRYSLER PACIFICA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V473000·2026-05-07
[pending] 2025 GRAND DESIGN LINEAGE
Pending LLM rewrite. Source: NHTSA 25V473000.
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
HighCPSC·26469·2026-05-07
Rublev Colours Gum Turpentine and Mineral Spirits Bottles Recalled
Natural Pigments is recalling about 860 bottles of Rublev Colours Gum Turpentine and Mineral Spirits due to non-compliant packaging that poses a risk of serious injury or death from child poisoning.
Product
Rublev Colours Gum Turpentine and Mineral Spirits Bottles
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-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 (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
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 (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

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