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 the agency’s own highest classification or reported deaths or serious injuries, 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

27401–27425 of 90165

HighFDA (Devices)·Z-0448-2022·2022-01-12
Orthopedic Inserter Shaft Recalled for Mating Incompatibility During Surgery
Flower Orthopedics is recalling 48 units of the Flex-Thread Inserter Shaft due to mating incompatibility with the Inserter Draw Rod. The defect may cause the draw rod to bind during fibula intramedullary nail insertion, potentially preventing surgery completion.
Product
Flex-Thread Inserter Shaft intended for Fibula intramedullary-intended to be used with the Inserter Draw Rod and Blue Ratchet Handle in order to facilitate the insertion of the Flex-Thread Nail System- Catalog Number: 8435-1
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22051·2022-01-12
2021 Giant and Liv Adult Bicycles Recalled for Loose Handlebar Stem
Giant Bicycle Inc. is recalling about 20,800 units of 2021 Model Year Giant and Liv adult bicycles because the adjustable handlebar stem can become loose, posing fall and injury hazards. The company has received 86 reports of loose handlebars, including three reports of riders falling.
Product
2021 Model Year Giant and Liv Adult Bicycles
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0459-2022·2022-01-12
Surgical Instrument Tray Recalled for Incorrect Keel Punch Component
Howmedica Osteonics Corp. is recalling Triathlon Pro Tibial Preparation Trays that may contain the wrong surgical instrument. The incorrect component could delay surgery or cause unintended bone preparation during knee replacement procedures.
Product
Triathlon Pro Tibial Preparation Tray, Revision AC- for organization, storage, and transport in preparation for sterilization of re-usable instruments required for implanting the Triathlon Globalization Implant System for individual patients receiving primary total knee…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0460-2022·2022-01-12
Abbott Alinity m System Molecular Diagnostic Device Amplification Defect Recall
Abbott Molecular is recalling 742 Alinity m System diagnostic devices worldwide due to potential for abnormal amplification curves that could affect test accuracy.
Product
Alinity m System, Part No. 08N53-002
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0464-2022·2022-01-12
Medtronic Abre Venous Stent System recalled for reports of stent migration
Medtronic is recalling the Abre Venous Self-Expanding Stent System due to reports of stent migration. Approximately 21,653 devices were distributed nationwide and internationally.
Product
Instructions for Use for all model numbers of the Medtronic Abre Venous Self-Expanding Stent System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0456-2022·2022-01-12
Hemodialysis Delivery System distributed without FDA premarket approval
The DBB-06 Hemodialysis Delivery System was distributed without required FDA premarket approval. Approximately 781 units were shipped to healthcare facilities in multiple states.
Product
DBB-06 Hemodialysis Delivery System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0447-2022·2022-01-12
Invacare AVIVA Storm RX Power Wheelchairs Recalled for Firmware Deceleration Malfunction
Invacare AVIVA Storm RX power wheelchairs with firmware version 6.1.2 may decelerate more aggressively than programmed, risking user injury.
Product
Invacare AVIVA Storm RX with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: SRX-20R, SRX-20SP, SRX-20MP
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·22V009000·2022-01-11
Oshkosh Recalls 2019-2022 S-Series Vehicles Due to Front Axle Bolt Failure Risk
Oshkosh is recalling 2019-2022 S-Series vehicles because front axle u-bolts may fail, potentially allowing the axle to shift or detach and increasing crash risk.
Product
OSHKOSH — OSHKOSH S-SERIES
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·22045·2022-01-11
Bella Residential Elevators Recalled for Child Entrapment Hazard
Bella residential elevators pose a risk of child entrapment between exterior and interior doors. Young children can become trapped and suffer serious injuries or death when the elevator moves to another floor.
Product
Bella residential elevators
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·22047·2022-01-11
Residential Elevators Recalled for Child Entrapment Hazard
Savaria and Garaventa residential elevators pose an entrapment risk to young children due to gaps between doors. Young children can become trapped and suffer serious injury or death when the elevator is called to another floor.
Product
Savaria and Garaventa branded residential elevators
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V007000·2022-01-11
Play-Mor Trailers Recalled Due to Propane Regulator Fire Risk
Play-Mor is recalling specific 2017-2020 trailers because a propane regulator may fail, increasing pressure and fire risk. Dealers will replace the parts free of charge.
Product
PLAY-MOR — PLAY-MOR MOTORSPORT SUV TRAILER, SINGLE ROOM TRAILER, 2 ROOM TRAILER, BBQ TRAILER
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·22046·2022-01-11
Inclinator residential elevators recalled for child entrapment hazard
Inclinator Company of America is recalling residential elevators manufactured from 1979 through 2021 because young children can become entrapped between the exterior landing door and interior elevator car door, risking serious injury or death.
Product
Inclinator residential elevators
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V008000·2022-01-11
Oshkosh Recalls 2019-2022 S-Series Vehicles Due to Fuel Leak Fire Risk
Oshkosh is recalling 2019-2022 S-Series vehicles because fuel tubes may crack, causing high-pressure leaks that increase fire risk.
Product
OSHKOSH — OSHKOSH S-SERIES
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V006000·2022-01-10
Reading Truck Recalls Marauder Dump Bodies Due to Weld Failure Risk
Reading Truck Body is recalling 2017-2021 Marauder Landscape Dump Body vehicles because a rear pivot mount weld may fail, increasing injury risk.
Product
READING TRUCK — READING TRUCK MARAUDER DUMP
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·003-2022·2022-01-08
Abbyland Foods Recalls Beef Sticks for Undeclared Milk Allergen
Abbyland Foods is recalling approximately 14,976 pounds of smoked beef sticks because they contain undeclared milk, a known allergen.
Product
Abbyland Foods, Inc. Recalls Beef Stick Product Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·22V005000·2022-01-07
Lakota Recalls 2021-2022 Trailers Due to Tire Belt Separation Risk
Lakota is recalling 2021-2022 Bighorn, Charger, and Livestock trailers because certain tires may experience belt separation, increasing crash risk.
Product
LAKOTA — LAKOTA BIGHORN, CHARGER, LIVESTOCK
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V003000·2022-01-07
2022 Forest River Aurora travel trailers recalled for furnace cooktop fire risk
Forest River is recalling 2021-2022 Aurora and Catalina travel trailers because the panel sealing the cooktop from the furnace was not properly sealed, which could cause an inverted flame and fire risk.
Product
COACHMEN — COACHMEN, FOREST RIVER CATALINA, AURORA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V004000·2022-01-07
2022 Forest River Cardinal Trailers Recalled for Tire Belt Separation
Forest River, Inc. is recalling certain 2021-2022 fifth wheel trailers equipped with defective Sailun tires that may experience belt separation. The defect could cause loss of vehicle control and increase the risk of a crash.
Product
PRIME TIME — PRIME TIME, FOREST RIVER, CONTINENTAL CARGO SANIBEL, CARDINAL, CRUSADER, CONTINENTAL CARGO
Category
Vehicle
Distribution
Distributed nationwide
CriticalUSDA FSIS·001-2022·2022-01-06
Interstate Meat Dist. Recalls Ground Beef Due To E. Coli O157:H7
Interstate Meat Dist. Inc. is recalling approximately 28,356 pounds of ground beef products due to possible E. coli O157:H7 contamination.
Product
Interstate Meat Dist. Inc., Recalls Ground Beef Products Due To Possible E. Coli O157:H7 Contamination
Category
Food
Distribution
Distributed nationwide
HighCPSC·22716·2022-01-06
Polaris Outlaw 110 EFI Youth ATVs Recalled for Fire Hazard
Polaris is recalling about 1,100 Model Year 2022 Outlaw 110 EFI Youth ATVs because the inner layer of the fuel line can leak, posing a fire hazard. No fires or injuries have been reported.
Product
Outlaw 110 EFI Youth All-Terrain Vehicles (ATVs)
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·002-2022·2022-01-06
Kettle River Recalls Chicken Alfredo Pizza for Undeclared Wheat Allergen
Kettle River Products is recalling approximately 1,464 pounds of chicken alfredo pizza due to misbranding and an undeclared wheat allergen. No adverse reactions have been reported.
Product
Kettle River Products Recalls Chicken Alfredo Pizza Products Due to Misbranding and an Undeclared Allergen
Category
Food
Distribution
Distributed nationwide
HighCPSC·22715·2022-01-06
Children's Covered Wood Wagons Recalled for Excessive Lead Paint
Colony Brands is recalling about 20 covered wood wagons sold through Montgomery Ward's and Ginny's from September to October 2021 because paint on the wood, plastic handles, and red plastic cover contains excessive lead that can be toxic if ingested by young children.
Product
Covered Wood Wagons
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0363-2022·2022-01-05
kleantouch Hand Sanitizer recalled for methanol contamination
Valisa MFG LLC is recalling kleantouch Hand Sanitizer 8 FL OZ pump bottles nationwide because the product contains methanol and was marketed without FDA approval. Consumers should stop using the product immediately.
Product
kleantouch HAND SANITIZER (ethyl alcohol 70%), 8.0 FL OZ (236 ML), pump bottles, Distributed by: Valisa MFG, LLC, Farmingdale, NY, 11735, Made in USA, UPC 6 86162 99246 1
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0323-2022·2022-01-05
SterRx Phenylephrine HCl Injection Recalled for Sterility Assurance
SterRx is recalling PHENYLephrine HCl 40 mg per 250 mL injectable solution nationwide due to lack of assurance of sterility. The recall affects approximately 20,640 bags distributed across the United States.
Product
PHENYLephrine HCl, 40 mg per 250 mL, (160 mcg per mL) in 0.9% Sodium Chloride Injection, Rx Only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-252-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0315-2022·2022-01-05
dilTIAZem HCl in Dextrose Injection Recalled for Sterility Assurance
SterRx is recalling dilTIAZem HCl in 5% Dextrose Injection due to lack of assurance of sterility. The recall affects 8,946 bags distributed nationwide.
Product
dilTIAZem HCl in 5% Dextrose Injection, 125 mg per 125 mL, (32 mcg per mL), Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-951-01.
Category
Drug
Distribution
Distributed nationwide

How to read this listing

Filters

27401–27425 of 90165