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

13926–13950 of 27735

HighFDA (Devices)·Z-1154-2024·2024-02-28
X-Ray C-Arm System Internal Board Defect Causes Abnormal Images
Canon Medical System X-ray C-arm systems may display abnormal images due to an internal board manufacturing defect, potentially preventing exam completion and requiring patients to be re-examined with alternative equipment.
Product
The device is an X-ray system that is capable of radiographic and fluoroscopic studies and is used in an interventional setting. The system consists of a C-arm which is equipped with an X-ray tube, beam limiter and X-ray receptor, X-ray controller, computers with system and proce
Category
Medical Device
Distribution
2 states
HighFDA (Drugs)·D-0326-2024·2024-02-28
Fluticasone Propionate Nasal Spray Recalled for Potential Bacterial Contamination
Apotex Corp. is recalling Fluticasone Propionate Nasal Spray (292,752 bottles nationwide) due to potential Burkholderia cepacia contamination from manufacturing deviations. No illnesses reported.
Product
FLUTICASONE PROPIONATE — FLUTICASONE PROPIONATE (FLUTICASONE PROPIONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0886-2024·2024-02-28
HARD E6 1036 bulk product recalled for foreign material contamination
Mennel Milling Company is recalling HARD E6 1036 bulk product distributed across six states due to potential contamination with metal, wood, gasket material, and sifter balls. No illnesses have been reported.
Product
HARD E6 1036 delivered as bulk product in approximately 50,000 lbs trailers
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-1147-2024·2024-02-28
Henry Schein Criterion Anti-Fog Earloop Masks Recalled for Equipment Validation Issue
AMD Medicom Inc. is recalling Henry Schein Criterion Anti-Fog Earloop Masks Level 3 (Blue) because the masks were produced on non-validated equipment not included in the product qualification process.
Product
HENRY SCHEIN¿ CRITERION¿ ANTI-FOG EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-3281)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0896-2024·2024-02-28
Wheat Flour Recalled for Potential Foreign Material Contamination
Mennel Milling Company is recalling bleached wheat flour due to potential contamination with metal, wood, gasket material, and sifter balls. The product was distributed across six states.
Product
BLEACHED WHEAT FLOUR 5600352 delivered as bulk product in approximately 50,000 lbs trailers
Category
Food
Distribution
6 states
HighFDA (Food)·F-0885-2024·2024-02-28
Mennel Milling Company Recalls Dried Grain Product for Foreign Material Contamination
Mennel Milling Company is recalling approximately 2.6 million pounds of DRIED SOFT 75 ENR 134348 due to potential contamination with metal, wood, gasket material, and sifter balls.
Product
DRIED SOFT 75 ENR 134348 delivered as bulk product in approximately 50,000 lbs trailers
Category
Food
Distribution
6 states
HighFDA (Food)·F-0912-2024·2024-02-28
Country Corner Dairy White Colby Cheese Recalled for Improper Pasteurization
Country Corner Dairy is recalling WHITE COLBY CHEESE products due to improper pasteurization. The recalled products were distributed to Maryland and Virginia.
Product
Fresh Local , Country Corner Dairy, WHITE COLBY CHEESE, INGREDIENTS: Pasteurized Milk, Salt , Rennet, Calcium Chloride, Cheese Culture, Contains Milk. Product comes in various sizes, 6 oz. up to 42 lbs. and is in vacuum sealed plastic packaging.
Category
Food
Distribution
2 states
HighFDA (Drugs)·D-0329-2024·2024-02-28
Meijer Cherry Cough Drops recalled for potential glass and silicone contamination
Bestco LLC is recalling Meijer Cherry Cough Drops due to potential glass and silicone particulates found during manufacturing quality control inspections. Consumers should stop using the product immediately.
Product
Meijer Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, 200 drops per bag, item number 20000345, Bestco, 288 Mazeppa Road, Mooresville, NC 28115
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1143-2024·2024-02-28
Ionolux dental cement recalled for manufacturing defect affecting curing
Ionolux dental cement capsules may contain incorrect plungers that prevent proper curing. Affected batches distributed in the US and internationally should not be used.
Product
Ionolux, Catalog (REF) Numbers: a) 2115, b)2117, c) 2118, d) 2119, e) 2120, f) 2122; dental cement
Category
Medical Device
Distribution
4 states
HighFDA (Food)·F-0884-2024·2024-02-28
Bread Flour Recalled for Potential Foreign Material Contamination
Mennel Milling Company is recalling bulk bread flour due to potential contamination with metal, wood, gasket material, and sifter balls. The flour was distributed to bakeries and food manufacturers in six states.
Product
BREAD FLOUR UNBL ENR delivered as bulk product in approximately 50,000 lbs trailers
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-1181-2024·2024-02-28
Radiation Oncology Treatment Planning Software VERIQA Calculation Error
PTW-FREIBURG's VERIQA software (versions 2.0 and 2.1) may incorrectly calculate gamma passing rates when users exclude voxels below a dose threshold, potentially displaying false positive dose evaluation results.
Product
Software VERIQA (S070031), version 2.0 and 2.1- Software package for display, evaluation and digital processing of medical image data sets and treatment plans in radiation oncology.
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1173-2024·2024-02-28
OPTIMIZER CCM X11 Implantable Pulse Generator May Fail to Deliver Therapy
The OPTIMIZER model CCM X11 implantable pulse generator may incorrectly detect a charging error and cease delivering cardiac therapy, potentially causing patients to experience heart failure symptoms. A total of 1,469 units are affected.
Product
OPTIMIZER model CCM X11 implantable pulse generator (IPG) devices - Smart Mini and Lite
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0890-2024·2024-02-28
Malted Flour Recalled for Potential Foreign Material Contamination
Mennel Milling Company recalls UNBLE ENR MALTED RM6144 FLOUR for potential foreign material contamination including metal, wood, gasket material, and sifter balls. The recall affects approximately 2.6 million pounds distributed in six states.
Product
UNBLE ENR MALTED RM6144 FLOUR delivered as bulk product in approximately 50,000 lbs trailers
Category
Food
Distribution
6 states
HighFDA (Food)·F-0904-2024·2024-02-28
Bulk Fortune Cookies Recalled for Undeclared Wheat and Soy
New World Company is recalling bulk cases of Fortune cookies distributed in California due to undeclared wheat and soy allergens that pose a risk to consumers with these allergies.
Product
Bulk case of Fortune cookies, labeled as 6 lb (1.3 lb per bag/ 4 bags per case)
Category
Food
Distribution
1 state
HighFDA (Drugs)·D-0347-2024·2024-02-28
Drug recall: CABTREO topical gel stored at improper temperature
CABTREO acne medication was stored outside refrigeration requirements. The recalled lot was kept at room temperature instead of required refrigerated conditions.
Product
CABTREO — CABTREO (CLINDAMYCIN PHOSPHATE/BENZOYL PEROXIDE/ADAPALENE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0878-2024·2024-02-28
Donut Cake Flour Recalled for Potential Metal and Foreign Material Contamination
Mennel Milling Company is recalling donut cake flour products due to potential contamination with metal, wood, gasket material, and sifter balls. The affected product was distributed across six states; no illnesses have been reported.
Product
1002560 DONUT CAKE FLR delivered as bulk product in approximately 50,000 lbs trailers
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-1148-2024·2024-02-28
Patterson Procedure Earloop Masks Recalled Due to Non-Validated Production Equipment
Patterson Procedure Earloop Masks (ASTM Level 3, blue) are being recalled because units were produced on non-validated equipment. The recall affects 180 cases with lot numbers 2339 and 2342, distributed across six states.
Product
PATTERSON¿ PROCEDURE EARLOOP MASKS- ANTI-FOG, ASTM LEVEL 3 (BLUE) (item code 127-7573)
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·24128·2024-02-22
MouTec Biometric Firearm Safes Recalled for Unauthorized Access Risk
The CPSC is recalling about 2,200 MouTec brand biometric firearm safes because the biometric lock can be opened by unauthorized users, posing a serious injury hazard and risk of death. One incident involved a 6-year-old opening the safe, though no injuries have been reported.
Product
MouTec brand Biometric Firearm Safes
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·24129·2024-02-22
Machir Biometric Personal Safes Recalled Due to Lock Failure Risk
Machir LLC recalled about 24,820 biometric personal safes because the biometric lock can fail and allow unauthorized access. The firm received 15 reports of the lock failing to secure safes, posing a serious injury hazard and risk of death if firearms are stored inside.
Product
Machir Biometric Personal Safes
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·24130·2024-02-22
Bulldog Biometric Firearm Safes Recalled Due to Lock Failure Risk
Bulldog Cases is recalling about 33,500 Magnum Biometric Pistol Vaults because the biometric lock can fail and be opened by unauthorized users, creating a serious injury hazard and risk of death when firearms are stored in the safe.
Product
Bulldog Biometric Firearm Safes
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24127·2024-02-22
Gun Safes with Failing Biometric Locks Recalled for Unauthorized Access Risk
About 60,000 Awesafe biometric gun safes can fail to lock, allowing unauthorized users to open them. No injuries reported, but consumers should immediately stop using the biometric feature and use the key instead until they receive a free replacement.
Product
Awesafe Biometric Gun Safes
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24739·2024-02-22
Spring Spirit and Biloban Pack and Play Mattresses Recalled for Suffocation Hazard
The CPSC has recalled Spring Spirit and Biloban pack and play mattresses sold on Amazon.com due to a suffocation hazard to infants. The mattresses violate federal safety regulations and lack required warnings and labels.
Product
Spring Spirit and Biloban Pack and Play Mattresses
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24738·2024-02-22
Magik & Kover Pack and Play Mattresses Recalled for Suffocation Hazard
Magik & Kover Pack and Play Mattresses sold on Amazon are being recalled because they violate federal safety regulations for crib mattresses and pose a suffocation hazard to infants. Consumers should immediately stop using the mattresses and contact the company for a refund.
Product
Magik & Kover Pack and Play Mattresses
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24124·2024-02-22
EVAS 20-lb Propane Exchange Cylinders Recalled for Fire Hazard
Worthington Enterprises is recalling about 146,160 EVAS 20-lb propane exchange cylinders that could leak gas and pose a fire hazard. Consumers should stop using them immediately and return them to AmeriGas for free replacement.
Product
EVAS 20-lb. propane exchange cylinders
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24123·2024-02-22
JURLEA Area Rugs Recalled for Fire Hazard Violation
About 230 JURLEA area rugs sold on Amazon violate federal flammability regulations and pose a fire hazard. No injuries have been reported. Consumers should stop using the rugs and contact the distributor for a refund.
Product
JURLEA Area Rugs
Category
Consumer Product
Distribution
Distributed nationwide

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13926–13950 of 27735