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

20401–20425 of 27461

HighFDA (Food)·F-0180-2023·2022-12-07
Amy's Kitchen Gluten Free Bean and Cheese Burritos Recalled for Plastic Contamination
Amy's Kitchen is recalling Gluten Free Bean and Cheese Burritos (Lot 30H0922, best before 08/2024) due to potential plastic pieces in the product. Approximately 5,134 cases were distributed to 18 U.S. states.
Product
Amy's Kitchen Gluten Free Bean and Cheese Burrito 5.5 oz. individually wrapped plastic packages - 12 units per case UPC - 042272-00353-2 Frozen INGREDIENTS: ORGANIC PINTO BEANS, FILTERED WATER, ORGANIC BROWN RICE, ORGANIC GARBANZO BEAN FLOUR, ORGANIC TOMATO PUR¿E, WHITE CHEDDAR A
Category
Food
Distribution
18 states
HighFDA (Drugs)·D-0071-2023·2022-12-07
Daytrana transdermal methylphenidate patches recalled for adhesive defect
Noven Pharmaceuticals recalls 3,977 boxes of Daytrana methylphenidate transdermal patches nationwide due to defective adhesive properties in lot 91316. Affected patches may fail to adhere properly or deliver medication inconsistently.
Product
DAYTRANA — DAYTRANA (METHYLPHENIDATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0324-2023·2022-12-07
CoViPoint COVID Test Kits Distributed Without FDA Approval or Clearance
GS Biomark LLC distributed approximately 639,200 CoViPoint COVID test kits without FDA approval, clearance, or authorization across multiple US states.
Product
CoViPoint COVID test kit (MultiPLEX/Direct) Kit Item Numbers: BC-DK0200; BM-AD4K0200 BM-ADK0200 BM-CDK0200 BM-CFDK0200 BM-D4K0200 BM-DK0200 BM-DK0600 BM-DK0800 BM-DK1200 BM-DK1400 BM-DK1800
Category
Medical Device
Distribution
11 states
HighFDA (Food)·F-0181-2023·2022-12-07
Fudgeamentals Chocolate Fudge Bites recalled for undeclared tree nuts
Fudgeamentals Chocolate Fudge Bites (8 oz) are being recalled because they contain undeclared tree nuts. Consumers with tree-nut allergies are at risk of allergic reaction.
Product
Fudgeamentals Chocolate Fudge Bites (8 oz); packaged in clear plastic container
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0343-2023·2022-12-07
Surgical Gown Recall Due to Potential Open Seal Pouches Affecting Sterility
Owens & Minor Distribution recalls Aero Blue Performance Surgical Gowns due to potential open seal pouches that could compromise sterility and result in non-sterile products being used in surgery.
Product
Aero Blue Performance Surgical Gown, XL- Sterile surgical gown Code: 41734
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-0340-2023·2022-12-07
Intuitive Da Vinci Stapler Instruments Recalled for Potential Staple Deployment Failure
Intuitive Surgical is recalling Da Vinci Xi surgical stapling instruments due to potential staple deployment failure and device fragment generation. No injuries have been reported.
Product
INTUITIVE Da Vinci Xi 8mm SureForm 30 Curved-Tip Stapler Da Vinci Xi|X REF 488530 INTUITIVE Da Vinci 8mm SureForm 30 Reload 30 mm Gray 4-Row 2.0 mm Xi|X REF 48230M INTUITIVE Da Vinci 8mm SureForm 30 Reload 30 mm White 4-Row 2.5 mm Xi|X REF 48230W INTUITIVE Da Vinci 8mm
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0346-2023·2022-12-07
Diagnostic Kit Recalled for False Positive Bacterial Identification Results
Accelerate Diagnostics is recalling the Accelerate PhenoTest BC kit due to improperly formulated FISH probes that produce false positive identification results for Staphylococcus aureus and Streptococcus species. Approximately 7,160 kits have been distributed across the United States and internationally.
Product
Accelerate PhenoTest BC kit REF 10102018
Category
Medical Device
Distribution
31 states
HighFDA (Devices)·Z-0347-2023·2022-12-07
Medical laboratory reagent recalled for potential false-negative test results
Greer Laboratories recalled a hypersensitivity pneumonitis test reagent (Lot 389591) due to decreased reactivity that could cause false-negative results. The issue affects 218 units distributed across 12 U.S. states and two countries.
Product
GREER M. FAENI, 0.25 mL 20 MG/ML, Item: K6, Analyte Specific Reagent, HYPERSENSITIVITY PNEUMONITIS test system, gel diffusion kit for demonstrating precipitating antibodies.
Category
Medical Device
Distribution
11 states
HighFDA (Devices)·Z-0344-2023·2022-12-07
Mobile CT Scanner Battery Fire Risk in Units With Bypassed Monitoring
Mobius Imaging is recalling MobiCT-32 AIRO Mobile CT Scanner units due to a reported battery fire in devices where battery monitoring systems were bypassed. The affected units' batteries must be replaced.
Product
MobiCT-32 AIRO Mobile CT Scanner, Cat. No. MobiCT-32, mobile computed tomography (CT) system, software version 2.1.1
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0354-2023·2022-12-07
Alcon Surgical Procedure Packs Recalled for Adhesive Defect and Skin Injuries
Alcon is recalling Custom Pak Surgical Procedure Packs because the adhesive liner is difficult to remove and the manufacturer has observed an increase in skin injuries related to the adhesive.
Product
Alcon Custom Pak Surgical Procedure Pack
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V896000·2022-12-06
Volvo Recalls 2022-2023 VNL Vehicles for Air Tank Bracket Defect
Volvo Trucks is recalling certain 2022-2023 VNL vehicles because excessively tightened air tank bracket fasteners may break, allowing the air tank to detach and become a road hazard.
Product
VOLVO — 2022 VOLVO VNL
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V900000·2022-12-06
KTM 1290 Super Duke R Motorcycles Recalled for Electrical Wiring Defect
KTM is recalling 2020-2022 1290 Super Duke R motorcycles because the main wiring harness may be misrouted or missing parts, potentially causing an electrical short-circuit and engine stall.
Product
KTM — 2020 KTM 1290 SUPER DUKE R
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·23055·2022-12-01
Gotway and Begode Unicycles Recalled for Fire Hazard
eWheels LLC is recalling about 500 Gotway and Begode electric unicycles because their lithium-ion batteries can ignite, creating a fire hazard. Fourteen fire incidents have been reported, including property damage and one injury.
Product
Gotway and Begode unicycles
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23715·2022-12-01
2022 Honda TRX90X ATVs Recalled Due to Stuck Throttle Cable
American Honda is recalling about 2,900 2022 model year TRX90X ATVs because the throttle cable can get stuck, creating a crash and injury hazard. Consumers should stop using the vehicles and contact an authorized Honda Powersports dealer for a free inspection and repair.
Product
2022 model year Honda TRX90X ATVs
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·23713·2022-12-01
Kubota RTV-XG850 Utility Vehicles Recall for Steering Shaft Failure
Kubota is recalling about 19,500 RTV-XG850 utility vehicles because the steering shaft can shear near the power steering housing, causing loss of steering control. No injuries or deaths have been reported.
Product
Kubota RTV-XG850 Model Utility Vehicles
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·23059·2022-12-01
JBR Solutions Recalls Aduro Surge Protectors for Shock and Fire Hazards
JBR Solutions is recalling about 51,750 Aduro surge protectors due to incorrect polarization and poorly soldered connections that pose shock and fire hazards. No injuries or fires have been reported.
Product
Aduro surge protectors
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23712·2022-12-01
Polaris RZR Pro XP 4 Vehicles Recalled Due to Fire Hazard
Polaris is recalling about 600 model year 2021-2022 RZR Pro XP 4 recreational off-road vehicles because a fuel leak at the fuel pump assembly joint can occur near a hot surface, creating a fire hazard. The company has received five reports of fuel leaks, including one report of fire, but no injuries have been reported.
Product
Model Years 2021-2022 RZR Pro XP 4 Recreational Off-Road Vehicles
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·23058·2022-12-01
The Laundress cleaning products recalled for bacterial contamination
The Laundress is recalling approximately 8 million laundry and household cleaning products that may contain harmful bacteria including Burkholderia cepacia complex, Klebsiella aerogenes, and Pseudomonas species. People with weakened immune systems or underlying lung conditions face risk of serious infection.
Product
The Laundress laundry and household cleaning products
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23714·2022-12-01
HABA USA Recalls Discovery Cubes Animal Hide and Seek Activity Toys
HABA USA is recalling about 800 Discovery Cubes Animal Hide and Seek activity toys because the seam on the toy's house can open, allowing access to filling that poses choking and ingestion hazards for young children. No injuries have been reported.
Product
Discovery Cubes Animal Hide and Seek Activity Toy
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23056·2022-12-01
Cuisinart Compact Blender and Juice Extractor Combos Recalled for Laceration Hazard
Conair is recalling about 66,000 Cuisinart Compact Blender & Juice Extractor Combos (Model CBJ-450) because the nut holding the blender blade assembly can loosen and detach during use, creating a laceration hazard.
Product
Cuisinart Compact Blender & Juice Extractor Combos Model CBJ-450
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0169-2023·2022-11-30
Tiramisu Twist Cookies recalled for undeclared tree nuts
DAISO CALIFORNIA WAREHOUSE is recalling Tiramisu Twist Cookie 3.4 oz. packages due to undeclared tree nuts. Consumers with tree nut allergies face allergic reaction risk if they consume this product unknowingly.
Product
Tiramisu Twist Cookie 3.4 oz. packaged in a gold bag with a large image of two cookies on the package. SKU 4562138450820 3.4 oz. packages, 12 units per case Product of Malaysia
Category
Food
Distribution
0 states
CriticalFDA (Food)·F-0174-2023·2022-11-30
Umami Everyday Sauce recalled for undeclared soy allergen
Umami Everyday Sauce is being recalled due to undeclared soy allergen. This poses a risk to consumers with soy allergies and sensitivities.
Product
Umami Everyday Sauce, 5 fl. oz. (148 mL) glass bottle, UPC 8-67732-00032-2, Made for Seed Ranch Flavor Co., LLC, Boulder, CO 80302 Ambient storage - minimum 35 degrees, maximum 85 degrees.
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0176-2023·2022-11-30
Everything But The Sushi & Dumplings sauce recalled for undeclared soy
Seed Ranch Flavor Co. is recalling Everything But The Sushi & Dumplings sauce due to undeclared soy allergen. Approximately 11,449 bottles were distributed nationwide and internationally.
Product
Everything But The Sushi & Dumplings, 5 fl. oz. (148 mL) glass bottle, UPC 8-60008-58851-7, Made for Seed Ranch Flavor Co., LLC Boulder, CO 80302. Ambient storage - minimum 35 degrees, maximum 85 degrees.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0263-2023·2022-11-30
3M Steri-Drape Surgical Drape Recall for Adhesive Defect and Skin Injuries
3M is recalling 554,200 surgical drapes due to a difficult-to-remove adhesive liner that may damage the product and render it unusable. The company has received reports of adhesive-related skin injuries from the affected lots.
Product
3M Steri-Drape, Medium Drape with Incise Film and Pouch, REF 1061NS, general surgery drape
Category
Medical Device
Distribution
0 states
SevereFDA (Food)·F-0173-2023·2022-11-30
Smoked Salmon Recalled Due to Possible Listeria Contamination
Wild caught Alaskan Sockeye smoked salmon may be contaminated with Listeria monocytogenes. Seven Seas International USA LLC is recalling 540 cases distributed to 164 retail stores.
Product
Wild caught Alaskan Sockeye Smoked Salmon NET WT 4 OZ (113g) EXPIRATION DATE 7-11-2024 UPC: 68826715832 Origin: USA, smoked and cured in The Netherlands
Category
Food
Distribution
0 states

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