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

23201–23225 of 26062

HighFDA (Food)·F-0366-2022·2022-01-19
Howling Cow Butter Almond Ice Cream recalled for undeclared allergens
Howling Cow Butter Almond ice cream sold in North Carolina and South Carolina contains Cookie Dough Ice Cream with undeclared soy and wheat allergens. Consumers with allergies should not consume the product.
Product
butter almond HOWLING COW THE ICE CREAM OF NC STATE UNIVERSITY One Pint (473 ml) Ingredients: Milk, Cream, Sugar, Almonds***Stabilizer***Carmel Color and Natural Flavor. Contains milk, almonds Proudly distributed by Hunter Farms High Point, NC 27262 UPC 0 74336 65079 6
Category
Food
Distribution
0 states
HighCPSC·22054·2022-01-19
FRIGG Silicone Pacifiers Recalled Due to Choking Hazard
Mushie & Co is recalling about 333,725 FRIGG Silicone Pacifiers because the silicone nipple can detach from the plastic shield, posing a choking hazard. Eight detachments have been reported in the U.S. with no injuries.
Product
FRIGG Silicone Pacifiers
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-0381-2022·2022-01-19
Bosket Bread Sourdough Bread Lacks Required Ingredient Statement
Bosket Bread Company is recalling sourdough bread products sold in Washington because packages are missing required ingredient statements, leaving consumers unable to identify potential allergens including wheat, milk, egg, soy, and sesame.
Product
Sourdough Bread, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0474-2022·2022-01-19
Computed Tomography System Software May Degrade Head Image Quality
Siemens SOMATOM Edge Plus CT systems running software version VB20_SP5 may produce degraded head images, potentially leading to patient misdiagnosis.
Product
SOMATOM Edge Plus-Computed tomography system Model 1026700
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0497-2022·2022-01-19
Vaxxen Labs Norexx Lean Mass Capsules Recalled for Undeclared Milk
NutraCap Labs is recalling Vaxxen Labs Norexx Lean Mass Agent Capsules (90ct bottle, UPC 0 612524 173315, Lot #2109041) because the product contains undeclared milk, which poses a risk to consumers with milk allergies.
Product
Vaxxen Labs Norexx Lean Mass Agent Capsules 90ct Bottle UPC CODE 0 612524 173315
Category
Consumer Product
Distribution
26 states
HighFDA (Food)·F-0396-2022·2022-01-19
Chili & Cheese Brat on Pretzel Bun Recalled for Undercooked Sausage
Kitchen Fresh Foods is recalling Chili & Cheese Brat on Pretzel Bun products because the sausage was not fully cooked. The recall affects 1,069 pieces distributed across multiple states.
Product
Chili & Cheese Brat on Pretzel Bun, Item Number 1098, Net Wt. 6.5 oz(185g), UPC 7 47804-01098 8. Keep Refrigerated. Packaged under the following brands: 1. Grabn'Go, MFG BY: KF Foods, Green Bay, WI 54313; 2. Fox River Vending Inc. Dst By: Fox River Appleton WI, 54
Category
Food
Distribution
6 states
HighNHTSA·22V016000·2022-01-18
2022 Peterbilt 579 chassis step bolts may loosen and cause injury
Bolts securing the chassis fairing step assembly on certain 2022 Peterbilt 579 vehicles may loosen and fracture. This can cause the step to move unexpectedly while entering or exiting the cab, increasing the risk of injury.
Product
PETERBILT — 2022 PETERBILT 579
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V015000·2022-01-17
2022 Keystone Alpine RV Exterior Ladder May Detach from Rear Wall
Keystone RV Company is recalling certain 2022 Alpine and Avalanche vehicles due to improperly secured exterior ladders that may detach while in use, creating a risk of injury.
Product
KEYSTONE — 2022 KEYSTONE ALPINE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V013000·2022-01-14
2021 Ford Diesel Trucks Fuel Filter Cap Defect Fire Risk
Ford is recalling certain 2021 diesel trucks due to a void in the secondary fuel filter cap that may leak fuel, posing a fire risk. Dealers will replace the fuel filters free of charge.
Product
FORD — 2021 FORD F-650
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V012000·2022-01-14
2022 Forest River Cherokee toy hauler tires may be incorrectly specified on placard
Forest River is recalling certain 2022 Cherokee toy haulers because the Tire and Loading Information placard may show incorrect rim specifications, potentially causing improper tire installation and crash risk.
Product
FOREST RIVER — 2022 FOREST RIVER CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0362-2022·2022-01-12
Godavari Brand Apricots Recalled for Undeclared Sulfites
Bokhary Foods, Inc. is recalling Godavari brand apricots in 7 oz and 14 oz packages because they contain undeclared sulfites. Consumers allergic or sensitive to sulfites should not consume the product.
Product
GODAVARI brand APRICOTS, packaged in 7 oz (UPC 0 03658 50001 4) and 14 oz (UPC 0 03657 5001 5) clear plastic-film bags with the GODAVARI brand label on the front. Each bag is filled with orange-colored dried apricots that can be seen through the bag.
Category
Food
Distribution
3 states
SevereFDA (Food)·F-0363-2022·2022-01-12
Nature's Own Honey Wheat Bread recalled for undeclared milk
Flowers Foods is recalling Nature's Own Honey Wheat Bread due to undeclared milk, which poses a risk to consumers with milk allergies. The product was distributed in Arizona, California, Colorado, New Mexico, Nevada, and Wyoming.
Product
Nature's Own Honey Wheat Bread, NET WT 20 oz (1LB 4 OZ) 567g, DISTRIBUTED BY FLOWERS BAKERIES, LLC THOMASVILLE, GA 31757 Single loaf UPC 0 72250 03706 8 & Double pack UPC 0 72250 00539 5
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-0458-2022·2022-01-12
UROMEDICA Implantation Instrument Sheath May Damage ProACT Implants
Uromedica is recalling nonsterile implantation instrument sheaths (Lot UM00794 and UM00817) because the U-channel sheaths may damage ProACT implant devices during implantation procedures. Affected devices were distributed nationwide.
Product
UROMEDICA Implantation Instrument Set (Sheath and Sharp Trocar), REF 750041, nonsterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0461-2022·2022-01-12
Alinity m System Software Issue Affects Maintenance and Diagnostics Procedures
Abbott Molecular is recalling 742 Alinity m System units worldwide due to a software issue that prevents Field Service Engineers from properly completing maintenance and diagnostics procedures.
Product
Alinity m System, Part No. 08N53-002
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0446-2022·2022-01-12
Invacare AVIVA FX power wheelchair LiNX Gyro deceleration malfunction
Some Invacare AVIVA FX power wheelchairs with LiNX Gyro firmware 6.1.2 may decelerate more aggressively than programmed, creating injury risk.
Product
Invacare AVIVA FX with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: IFX-20R, IFX-20SP, IFX-20MP, IFX-20C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0455-2022·2022-01-12
COVID-19 Diagnostic Kit Recall for Inaccurate Test Results
Qiagen Sciences is recalling 376 units of its QIAstat-Dx Respiratory SARS-CoV-2 Panel diagnostic kit due to faulty cartridges that can produce false-negative or false-positive test results.
Product
QIAstat-Dx Respiratory SARS-CoV-2 Panel (US IVD under FDA EUA 200075); REF 691223
Category
Medical Device
Distribution
9 states
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
HighFDA (Devices)·Z-0445-2022·2022-01-12
Power wheelchairs with LiNX Gyro module recalled for deceleration control failure
Invacare power wheelchairs with LiNX Gyro firmware 6.1.2 may decelerate more aggressively than programmed, risking user injury due to an incorrect deceleration profile.
Product
Invacare TDX SP2 with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: TDX SP2: TDXSP2, TDXSP2-CG, TDXSP2X-CG, TDXSP2-MCG, TDXSP2X-MCG, TDXSP2V, TDXSP2V-HD, TDXSP2HD, TDXSP2HD-CG, TDXSP2HD-MCG
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-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
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 arthropl
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
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 (Food)·F-0503-2022·2022-01-12
Macaroni & Cheese Recalled Due to Undeclared Egg Allergen
Sandridge Food Corporation is recalling Macaroni & Cheese (Macarrones con Queso) distributed to restaurants and a hotel in Texas because the product contains egg but does not declare this allergen on the label.
Product
Macaroni & Cheese, Macarrones con Queso; 3-5 lb pouches/bolsas, NET WT/PESO NETO 240 OZ (15 LB) 6.80 kg; distributed by Gordon Food Service, Reorder No. 540061, Vendor Item # 4357505, Perishable. Keep Refrigerated. Perecedero. Mantener Refrigerado.
Category
Food
Distribution
0 states

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23201–23225 of 26062