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.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

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

19201–19225 of 27466

HighFDA (Food)·F-0394-2023·2023-03-08
Drizzilicious Mini Rice Cake Bites Recalled for Undeclared Peanut Residue
Snack Innovations Inc. is recalling Drizzilicious Mini Rice Cake bites due to undeclared peanut residue that may be present. Consumers with peanut allergies are at risk.
Product
Drizzilicious Mini Rice Cake bites Net Wt. 4oz and/or .74oz Bags Cookies & Cream UPC: 857900005167 and 857900005181 Packaged in a plastic bags Product also packed in the Drizzilicious mini rice cakes 32-ct Variety box
Category
Food
Distribution
10 states
HighFDA (Drugs)·D-0406-2023·2023-03-08
FDA Recalls Rosuvastatin Tablets Due to Manufacturing Practice Deviations
Accord Healthcare is recalling Rosuvastatin 20 mg tablets distributed in the US, Puerto Rico, and Canada due to Current Good Manufacturing Practice (CGMP) deviations. The deviations could affect product quality and safety.
Product
ROSUVASTATIN — ROSUVASTATIN (ROSUVASTATIN)
Category
Drug
Distribution
0 states
HighFDA (Food)·F-0392-2023·2023-03-08
Drizzilicious Mini Rice Cake Bites Recalled for Undeclared Peanut Residue
Snack Innovations Inc. is recalling Drizzilicious Mini Rice Cake bites for undeclared peanut residue. The recall affects approximately 6,701 cases distributed across multiple states; consumers with peanut allergies should not consume the product.
Product
Drizzilicious Mini Rice Cake bites Net Wt. 4oz and .74oz Bags Birthday Cake UPC: 857900005402 and 857900005419 Packaged in a plastic bags Product also packed in the Drizzilicious mini rice cakes 32-ct Variety box
Category
Food
Distribution
10 states
HighFDA (Drugs)·D-0388-2023·2023-03-08
Doxazosin tablets recalled due to manufacturing quality control deviations
Accord Healthcare is recalling 75,190 bottles of Doxazosin 4 mg tablets due to manufacturing quality control deviations discovered during an FDA inspection. No illnesses have been reported.
Product
DOXAZOSIN — DOXAZOSIN (DOXAZOSIN)
Category
Drug
Distribution
0 states
HighFDA (Drugs)·D-0424-2023·2023-03-08
Pravastatin Sodium 80 mg tablets recalled for manufacturing deviations
Accord Healthcare is recalling Pravastatin Sodium 80 mg tablets due to manufacturing process deviations discovered during an FDA inspection. The recall affects approximately 1,970 bottles distributed in the United States, Puerto Rico, and Canada.
Product
PRAVASTATIN SODIUM — PRAVASTATIN SODIUM (PRAVASTATIN SODIUM)
Category
Drug
Distribution
0 states
HighFDA (Devices)·Z-1185-2023·2023-03-08
Medivac Guardian blood loss estimation device inserts may provide inaccurate readings
Stryker's Medivac Guardian 3L scanning labels may cause inaccurate blood loss estimates, potentially delaying treatment for postpartum hemorrhage. The recall affects 541 units distributed nationwide.
Product
Finished Goods Box of 50 Inserts and Scanning Labels for Medivac Guardian 3L Catalog Number: FG 12022. Intended adjunct in the estimation of blood loss.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1193-2023·2023-03-08
Medical Device Recall: Vascular Diagnostic Device Air Embolism Risk
Unetixs Vascular is recalling 1706 units of the MultiLab Series II 2CP & 2CP Express vascular diagnostic device due to luer fittings that could allow air lines to be misconnected to intravenous lines, potentially causing air embolism.
Product
MultiLab Series II 2CP & 2CP Express non-invasive vascular diagnostic device, Model Number 11996-0000-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1191-2023·2023-03-08
Stryker Hoffmann LRF Transport Strut Locking Mechanism Recall
Stryker is recalling Hoffmann LRF Transport Strut devices due to oversized thread pitch that prevents the distal ring fixation from locking, affecting 488 units nationwide.
Product
stryker Hoffmann LRF, Transport Strut, Model Number 4933-0-400; Orthopedic external fixation device intended to keep bone fragments/segments in a correct anatomical position until reliable bone consolidation is achieved
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0425-2023·2023-03-08
Ropinirole tablets recalled due to FDA manufacturing compliance deviations
Accord Healthcare recalls 139,332 bottles of ropinirole 0.25 mg tablets distributed in the US, Puerto Rico, and Canada due to manufacturing compliance deviations identified during FDA inspection.
Product
ROPINIROLE — ROPINIROLE (ROPINIROLE)
Category
Drug
Distribution
0 states
HighFDA (Devices)·Z-1188-2023·2023-03-08
Maquet CARDIOHELP System extracorporeal support device components recalled for sterility
Maquet is recalling CARDIOHELP System components due to insufficient evidence of packaging sterility. Non-sterile medical devices could expose patients to infection, sepsis, or ischemia.
Product
BEQ-HLS 5050 USA; HLS Set Advanced 5.0, Product Code 70106.9077, BEQ-HLS 7050 USA; HLS Set Advanced 7.0, Product Code 70106.9078. Part of the CARDIOHELP System, a pre-connected set used for extracorporeal respiratory and/or cardiovascular support.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V149000·2023-03-07
Kia K5 side curtain air bags may not deploy in crash
Kia is recalling 2021-2023 K5 vehicles due to potentially incorrect installation of side curtain air bags that could prevent proper deployment in a crash.
Product
KIA — 2022 KIA K5
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V151000·2023-03-07
2023 Grand Design Imagine Travel Trailers Recalled for Incorrect Tire Specification Label
Grand Design is recalling 139 units of 2023 Imagine travel trailers. The Federal Certification Label incorrectly states tire size and inflation pressure, which may cause premature tire wear or blowout, increasing crash risk.
Product
GRAND DESIGN — 2023 GRAND DESIGN IMAGINE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V146000·2023-03-06
2023 Triumph Bonneville T120 motorcycles recalled for brake disc detachment risk
Triumph is recalling certain 2023 Bonneville T120 motorcycles because the left-hand side brake disc may detach, reducing brake performance and increasing crash risk. Dealers will install replacement parts free of charge.
Product
TRIUMPH — 2023 TRIUMPH BONNEVILLE T120
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V143000·2023-03-03
2023 Mack Granite Trucks Recalled for Loose Axle Fasteners
Mack is recalling approximately 17 model-year 2023 Granite trucks because front-drive steer axle fasteners may not have been properly tightened and could come loose, risking loss of steering control and crashes.
Product
MACK — 2023 MACK GRANITE (GR)
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V142000·2023-03-03
2023 Toyota Tundra Hybrid Tonneau Cover May Detach While Driving
Toyota is recalling 2022-2023 Tundra and Tundra Hybrid trucks with Toyota genuine tonneau covers. The cover's attachment joints may loosen and allow the cover to detach while driving, creating a road hazard.
Product
TOYOTA — 2023 TOYOTA TUNDRA HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·23138·2023-03-02
Patagonia Infant Capilene Base Layer Sets Recalled for Choking Hazard
Patagonia is recalling about 8,000 Infant Capilene Midweight Base Layer Sets because snaps on the bodysuit can detach, posing a choking hazard to infants. One incident of a snap detaching and being mouthed by a baby has been reported.
Product
Infant Capilene Midweight Base Layer Sets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23137·2023-03-02
TJX Office Chairs Recalled Due to Fall Hazard
The TJX Companies is recalling approximately 81,700 office chairs because the back can break or detach from the seat base when occupied, posing a fall hazard. The firm has received 12 reports of the chair back failing, including 10 reports of injuries.
Product
Office Chairs
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23141·2023-03-02
Helly Hansen Adult Workwear Sweatshirts and Hoodies Recalled for Burn Hazard
Helly Hansen is recalling about 13,900 adult workwear sweatshirts and hoodies because they fail to meet federal flammability standards for clothing textiles, posing a risk of burn injuries.
Product
Adult workwear sweatshirts and hoodies
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·23V140000·2023-03-02
2023 Winnebago Adventurer, Vista, Sunstar motorhomes recalled for missing rear reflectors
Winnebago is recalling certain 2023 Adventurer, Vista, and Itasca Sunstar motorhomes for missing rear reflectors that fail federal safety standards. Missing reflectors reduce visibility to other drivers, increasing crash risk.
Product
WINNEBAGO — 2023 WINNEBAGO ADVENTURER
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·23140·2023-03-02
RELiON InSight Series Lithium Batteries Recalled for Thermal Burn and Fire Risk
RELiON Battery is recalling certain lots of InSight Series 48V lithium-ion batteries because they can overheat, posing thermal burn and fire hazards. The company has received five reports of overheating with no injuries reported to date.
Product
RELiON InSight Series® lithium batteries
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·23V138000·2023-03-02
Newmar Motorhome Entry Door Latch May Fail, Preventing Emergency Exit
Newmar is recalling certain 2021-2023 Bay Star, Bay Star Sport, and Canyon Star motorhomes because the entry door latch may fail and prevent entry or exit, increasing the risk of injury in emergencies.
Product
NEWMAR — 2023 NEWMAR BAY STAR
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·23731·2023-03-02
Classic Whimsy Children's Pajamas Recalled for Flammability Standard Violation
Smocked Runway is recalling about 7,200 Classic Whimsy children's pajamas that fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries. Consumers should stop using the product immediately and contact the manufacturer for return instructions.
Product
Classic Whimsy children's pajamas
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23730·2023-03-02
Multi-Purpose Kids Bike Helmets Recalled for Head Injury Risk
Ouwoer Kids Bike Helmets sold on Amazon from March to November 2022 fail to meet federal safety standards and may not protect children in a crash. About 120 units are affected; no injuries have been reported.
Product
Multi-Purpose Kids Bike Helmets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23139·2023-03-02
Primark Children's Bamboo Plates Recalled for Lead and Formaldehyde
Primark is recalling about 1,665 children's bamboo plates sold from October 2021 through August 2022 because they contain elevated levels of lead and formaldehyde, which are toxic if ingested by children.
Product
Children's Bamboo Plates
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0371-2023·2023-03-01
Harvest Biscuits recalled for undeclared soy and peanut allergens
Harvest Biscuits 4Kinds of Nuts (94g units) are recalled because the product contains soy and peanuts that are not listed on the ingredient label. The product was distributed to Daiso stores across multiple US states and Canada.
Product
Harvest Biscuits 4Kinds of Nuts 94g units UPC:4901940041558
Category
Food
Distribution
5 states

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19201–19225 of 27466