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

22876–22900 of 90089

HighFDA (Food)·F-0078-2023·2022-11-02
The Chai Box Chai Concentrate Recalled for Potential Clostridium Botulinum Contamination
The Chai Box is recalling chai concentrate due to potential Clostridium botulinum contamination. Product testing revealed a pH level of 4.9, which creates conditions supporting bacterial growth.
Product
THE CHAI BOX CHAI CONCENTRATE 16FL OZ/473ML glass bottles UPC 7 93611 81925 2 REGRIGERATE AFTER OPENING. USE WITHIN 14 DAYS and 64FL OZ/1892ML plastic bottles KEEP REFRIGERATED USE WITHIN 7 DAYS OF OPENING UPC 7 93611 81926 9. INGREDIENTS Water, Black Teas, Spices - Cardamom…
Category
Food
Distribution
50 states
HighFDA (Devices)·Z-0128-2023·2022-11-02
ConvaTec Esteem+ Durahesive Plus Ostomy Pouch Release Liner Defect
ConvaTec recalled 182 units of Esteem+ Durahesive Plus ostomy pouches nationwide due to impaired release liner functionality. The defect affects pouches with batch number 2A02671 and UDI 768455115334.
Product
ConvaTec Esteem+ Durahesive Plus, Drainable Pouch, 3/4-2 1/4 in., 19-64mm, REF 416975. For the management of stoma output following a colostomy or ileostomy procedure.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22E093000·2022-11-02
ITR Recalls Oasis Chinook Hydronic Heaters Due to Fuel Line Defect
International Thermal Research is recalling Oasis Chinook Hydronic Heaters because an air line may be installed instead of a fuel line, creating a fire risk.
Product
FUEL SYSTEM, DIESEL:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V858000·2022-11-02
2021 Volkswagen ID.4 Passenger Air Bag May Fail to Deploy Properly
Volkswagen is recalling certain 2021 ID.4 vehicles because the passenger air bag may be incorrectly folded and could fail to protect occupants during a crash.
Product
VOLKSWAGEN — VOLKSWAGEN ID.4
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0130-2023·2022-11-02
ConvaTec Ostomy Pouch Recalled for Impaired Release Liner Functionality
ConvaTec is recalling 2,611 units of its Active Life ostomy pouch due to impaired release liner functionality. The defect may affect product performance and seal integrity.
Product
ConvaTec Active Life, One-Piece Drainable Pouch, 3/4-2 1/2 in., 19-64mm, REF 400599. For the management of stoma output following a colostomy or ileostomy procedure.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0127-2023·2022-11-02
ConvaTec Esteem+ Durahesive Plus ostomy pouches recalled for release liner defect
ConvaTec is recalling 5,284 units of Esteem+ Durahesive Plus ostomy pouches due to impaired release liner functionality. The defect may affect proper device operation for patients managing colostomy or ileostomy output.
Product
ConvaTec Esteem+ Durahesive Plus, Drainable Pouch, 3/4-2 1/2 in., 19-64mm, REF 416976. For the management of stoma output following a colostomy or ileostomy procedure.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0073-2023·2022-11-02
Indian Gooseberry Extract Recalled for Elevated Lead Levels
Secrets of the Tribe is recalling Indian Gooseberry Alcohol-Free Extract (2 oz and 4 oz bottles) distributed nationwide due to elevated lead levels. Consumers should stop using the product.
Product
Indian Gooseberry Alcohol-Free Extract, 2 oz. glass bottle, UPC 722267094379 and Indian Gooseberry Alcohol-Free Extract, 4 oz. glass bottle, UPC 722267094393, Secrets of the Tribe LLC, PO Box 5264, Denver, CO, 80217
Category
Food
Distribution
Distributed nationwide
HighNHTSA·22V820000·2022-11-02
2023 BMW X5 and X7 Windshield Bonding Defect Poses Fire Risk
BMW is recalling 2023 X5 and X7 models with windshield bonding defects that may allow water to enter the vehicle and cause an electrical short-circuit, increasing fire risk.
Product
BMW — BMW X7, X5
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0016-2023·2022-11-02
Proton Armor hand sanitizer recalled for methanol contamination
Ultra Chem Labs Corp is recalling Proton Armor hand sanitizer nationwide due to trace amounts of methanol found in a manufacturing component. No illnesses have been reported.
Product
Proton Armor, Anti-Microbial Alcohol-Free Foaming Hand Sanitizer, kills 99.99% of germs, Odor Free, Family Safe, No Gels, Water Based, 24 Hour Germ Protection with Moisturizers for Sensitive Skin, a) 8 oz bottle, b) 32 oz bottle and c) 1.7 fl oz or 50 mL bottle, Supplier…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0136-2023·2022-11-02
GORE CARDIOFORM ASD Occluder Cardiovascular Implants Recalled for Manufacturing Test Failure
W L Gore & Associates is recalling 98 GORE CARDIOFORM ASD Occluder cardiovascular implants due to failed manufacturing release test results. Affected units were distributed nationwide and internationally.
Product
GORE CARDIOFORM ASD Occluder. cardiovascular implant.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0118-2023·2022-11-02
AutoPulse Resuscitation System Battery Recalled for Increased Li-ion Failures
ZOLL Circulation is recalling 6,353 AutoPulse Li-ion Batteries used in the AutoPulse Resuscitation System Model 100 CPR device due to an increase in battery failures. Affected users should contact the manufacturer for replacement guidance.
Product
AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model 100. used as an adjunct to manual CPR
Category
Medical Device
Distribution
48 states
HighFDA (Devices)·Z-0134-2023·2022-11-02
ARIES SARS-CoV-2 Assay Recalled Due to Syringe Defect
Luminex is recalling certain lots of the ARIES SARS-CoV-2 Assay because a defect in the wash 1 syringe could cause incomplete sample extraction and produce false negative test results.
Product
ARIES SARS-CoV-2 Assay, REF: 50-10047
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0017-2023·2022-11-02
Proton Armor Hand Sanitizer Recalled Due to Methanol Contamination
Ultra Chem Labs Corp is recalling Proton Armor Anti-Microbial Alcohol-Free Foaming Hand Sanitizer nationwide due to trace amounts of methanol found in product components during manufacturing. The recall affects multiple bottle sizes with batch number 20117206.
Product
Proton Armor, Anti-Microbial Alcohol-Free Foaming Hand Sanitizer, kills 99.99% of germs, Green Tea and Aloe, Family Safe, No Gels, Water Based, 24 Hour Germ Protection with Moisturizers for Sensitive Skin, a) 8 oz bottle, b) 32 oz bottle, and c) 1.7 fl oz or 50 mL bottle…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0020-2023·2022-11-02
Fondaparinux Sodium Injection Recalled Nationwide for Subpotent Formulation
AuroMedics Pharma LLC is recalling 11,520 units of Fondaparinux Sodium Injection nationwide due to out-of-specification potency. Patients should contact their healthcare provider immediately.
Product
FONDAPARINUX SODIUM — FONDAPARINUX SODIUM (FONDAPARINUX SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0072-2023·2022-11-02
Secrets of the Tribe Amla Alcohol-Free Extract recalled for elevated lead
Secrets of the Tribe is recalling Amla Alcohol-Free Extract (2 oz and 4 oz bottles) distributed nationwide due to elevated lead levels.
Product
Amla Alcohol-Free Extract, 2 oz. glass bottle, UPC 041979376093 and Amla Alcohol-Free Extract, 4 oz. glass bottle, UPC 041979376116, Secrets of the Tribe LLC, PO Box 5264, Denver, CO, 80217
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0139-2023·2022-11-02
Stryker INBONE Tibial Tray Recalled Due to Oversized Lock Detail
Stryker INBONE Tibial Trays are being recalled due to an oversized lock detail that could affect proper component assembly and implant function. Affected units were distributed in New York.
Product
Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 16mm Stem Base, REF 200252903, Size 3
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0137-2023·2022-11-02
CorVocet Biopsy System recalled for needle ejection risk from component misalignment
Merit Medical Systems is recalling CorVocet Biopsy Systems due to manufacturing defects that may cause the needle to eject when triggered outside the body, risking needle stick injuries to users or patients.
Product
CorVocet Biopsy System/Catalog Code: CORA1610/B, CORA1610S/B, CORA1615/B, CORA1810/A, CORA1810/B, CORA1810S/B, CORA1815/A, CORA1815/B, CORA1815S/A, CORA1815S/B, CORA1820/A, CORA1820/B, CORA1820S/A, CORA1825/A, CORA1825/B, CORA1825S/A, CORA2010/A, CORA2010/B, CORA2010S/A…
Category
Medical Device
Distribution
42 states
HighFDA (Devices)·Z-0125-2023·2022-11-02
Hip Liner Implants Mixed with Knee Inserts in Packaging
Encore Medical is recalling EMPOWR hip liner implants because boxes may contain knee inserts instead. This packaging error could delay surgeries. Four units affected in six US states.
Product
EMPOWR Acetabular System, Liner, 10 deg Hooded, HXe+ 40H, REF: 942-01-40H. Orthopedic implant component.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0077-2023·2022-11-02
Qassim Mix for Coffee Recalled Due to Undeclared Milk Allergen
Tomoorona LLC is recalling Qassim Mix for Coffee due to undeclared milk in the label. The product contains sodium caseinate (a milk derivative) but does not warn consumers about milk allergen, risking harm to those with milk allergies.
Product
Qassim Mix for Coffee, Net Weight 125g, packaged in a plastic container (UPC 6-281103 300011). Each case contains 48-125g containers.
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-0131-2023·2022-11-02
LINEAR Intra-Aortic Balloon Catheter Recalled for Incorrect Volume Labeling
Datascope's LINEAR intra-aortic balloon catheter has an incorrect balloon volume label on internal instructions that may delay critical therapy in unstable patients.
Product
LINEAR 7.5Fr. 40cc IAB with Accessories (APA), Model No. 0684-00-0480-02. intra-aortic balloon catheter.
Category
Medical Device
Distribution
0 states
SevereNHTSA·22V817000·2022-11-01
Brake modulator corrosion recall on Freightliner and Western Star commercial trucks
Daimler Trucks North America is recalling certain Freightliner Cascadia and Western Star models due to corrosion in front brake modulator valves. The defect may cause brakes to pull to one side during automated braking, increasing crash risk.
Product
FREIGHTLINER — FREIGHTLINER, WESTERN STAR CASCADIA, BUSINESS CLASS M2, 49X, 114SD
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V818000·2022-11-01
2017-2021 Tesla Model S and Model X power steering assist loss
Tesla is recalling 2017-2021 Model S and Model X vehicles due to power steering assist failure on rough roads or after hitting potholes, which increases crash risk.
Product
TESLA — TESLA MODEL S, MODEL X
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22E092000·2022-11-01
Tesla 2021 Model S Rearview Mirrors Recalled for Visibility Defect
Tesla is recalling 2021 Model S exterior rearview mirrors that do not meet federal rear-visibility standards. Defective mirrors may cause drivers to misjudge vehicle distances, raising crash risk.
Product
TESLA — TESLA MODEL S
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V816000·2022-10-31
2021 Hyundai Santa Fe Hybrid seat belt pretensioners may explode in crash
Hyundai is recalling 2021-2023 Santa Fe Hybrid and 2022-2023 Santa Fe Plug-In Hybrid vehicles, plus 2023 Genesis G80 Electric vehicles, because seat belt pretensioners may explode in a crash and project metal fragments. Dealers will secure the pretensioners with a cap at no cost.
Product
GENESIS — GENESIS, HYUNDAI G80 ELECTRIFIED, SANTA FE HYBRID, SANTA FE PLUG-IN HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V813000·2022-10-31
Forest River Recalls Fifth Wheels Due to Holding Tank Retention Defect
Forest River is recalling specific 2019-2022 fifth wheels because a cross-member may fail to retain holding tanks, increasing crash risk.
Product
COACHMEN — COACHMEN, SHASTA CHAPARRAL, PHOENIX, BROOKSTONE, CHAPARRAL LITE
Category
Vehicle
Distribution
Distributed nationwide

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22876–22900 of 90089