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

13901–13925 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-0348-2024·2024-02-28
Clobazam tablets recalled nationwide for residual solvent deviation
Micro Labs Limited is recalling 24,768 bottles of Clobazam 10mg tablets nationwide due to out-of-specification residual solvents. Patients should contact their healthcare provider for guidance.
Product
CLOBAZAM — CLOBAZAM (CLOBAZAM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1178-2024·2024-02-28
Azurion 7 Medical Imaging System May Lose Power During Procedures
Philips Azurion 7 imaging systems may experience power loss due to a potential short circuit in the power inverter, risking delays or termination of diagnostic and surgical procedures.
Product
Azurion 7 with a Certeray generator-To perform image guidance in diagnostic, interventional, and minimally invasive surgery procedures Models: (1) 722223, (2) 722224, (3) 722225, (4) 722226
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1151-2024·2024-02-28
Philips Allura Xper X-ray systems disk bay component may malfunction
Philips has recalled certain Allura Xper interventional X-ray systems because the disk bay component may fail, potentially preventing system operation and imaging procedures.
Product
Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of affected systems. Affected PCs: Imaging Processing PC, Host PC, FlexVision PC Allura Xper Model Name - Model Number: Allura Xper FD10 722003 722010 722026;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0898-2024·2024-02-28
Hard Wheat Flour Recalled for Potential Metal and Wood Contamination
Mennel Milling Company is recalling hard wheat flour distributed in six states due to potential contamination with metal, wood, gasket material, and sifter balls. Approximately 2.6 million pounds of product may be affected.
Product
HARD WHEAT 2ND CLEAR delivered as bulk product in approximately 50,000 lbs trailers
Category
Food
Distribution
6 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-0900-2024·2024-02-28
Bulk Animal Feed Recalled for Potential Foreign Material Contamination
Mennel Milling Company is recalling non-human consumption feed products due to potential contamination with metal, wood, and gasket material. Approximately 2.6 million pounds were distributed across six states.
Product
NON-HUMAN CONSUMPTION delivered as bulk product in approximately 50,000 lbs trailers
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-1179-2024·2024-02-28
Biliary Endoprosthesis Labeling Mismatch Risks Incorrect Device Placement
W.L. Gore's GORE VIABIL Short Wire Biliary Endoprosthesis may be mislabeled regarding drainage holes, risking extended procedures, infections, and unplanned device removal in 24 units distributed in Georgia.
Product
GORE VIABIL Short Wire Biliary Endoprosthesis, Product labeled as (1) Catalog Number VSWVH1008, 10 mm x 8 cm; with holes; and (2) Catalog Number VSWVN1008, 10 mm x 8 cm; no holes
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0881-2024·2024-02-28
Bulk animal feed product recalled for potential foreign material contamination
Mennel Milling Company is recalling 2ND CLEAR 1051664, a bulk animal feed product, due to potential contamination with metal, wood, gasket material, and sifter balls. Affected products were distributed in Kentucky, Michigan, New Jersey, New York, Ohio, and Pennsylvania.
Product
2ND CLEAR 1051664 delivered as bulk product in approximately 50,000 lbs trailers
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-1145-2024·2024-02-28
Philips Azurion Interventional X-ray Systems framegrabber card may fail to display images
The framegrabber card in Philips Azurion interventional X-ray systems may fail to display diagnostic images properly, potentially delaying procedures.
Product
Philips Azurion Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of the affected system. Affected PCs: FlexViewing PC Azurion Model Name - Model Number: Azurion 7 B12 722067; Azurion 7 B20 722068; Azurion 7 M12 722078 722223;
Category
Medical Device
Distribution
Distributed nationwide
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 (Drugs)·D-0341-2024·2024-02-28
FDA Recalls TERLIVAZ Terlipressin Due to Temperature Excursion During Shipping
Mallinckrodt recalls TERLIVAZ (terlipressin) injection due to temperature excursion during shipping. A cGMP deviation may compromise drug stability.
Product
TERLIVAZ — TERLIVAZ (TERLIPRESSIN)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1167-2024·2024-02-28
ESG Cutting Forceps Jaw May Fracture During Use or Inspection
Olympus Corporation of the Americas is recalling ESG PK Cutting Forceps because the jaw may fracture during pre-procedure inspection or during the procedure, posing a potential injury risk.
Product
ESG PK CUTTING FORCEPS, 5MM, 33CM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1155-2024·2024-02-28
X-ray fluoroscopy system may display abnormal images due to detector board defect
Canon Medical's INFX-8000F X-ray system may display abnormal horizontal stripe patterns due to a manufacturing change in the flat panel detector's internal board, potentially preventing exam completion.
Product
The INFX-8000F is designed to take advantage of the latest technological innovations to reduce dose and to save time. A revolutionary graphic user interface and a multi-tasking computer enable the system to fully meet the requirement for optimum image quality, safety, ease of use
Category
Medical Device
Distribution
2 states
HighFDA (Food)·F-0905-2024·2024-02-28
Fortune Cookies Recalled Due to Undeclared Soy Allergen
Fortune cookies from New World Company are recalled for containing undeclared soy allergen. The 1 lb retail bags were distributed in California to consumers.
Product
Fortune cookies, 1 lb plastic retail bags
Category
Food
Distribution
1 state
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 (Food)·F-0877-2024·2024-02-28
Mennel Milling White Flour Recalled for Potential Foreign Material
Mennel Milling Company is recalling white flour delivered as bulk product due to potential contamination with metal, wood, gasket material, and sifter balls. The recall affects approximately 2.6 million pounds distributed across six states.
Product
1000000 White Flour UNBL EN MT delivered as bulk product in approximately 50,000 lbs trailers
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-1172-2024·2024-02-28
Synapse CV 6 Imaging Software Calculation Error May Cause Misdiagnosis
FUJIFILM Synapse CV 6 medical imaging software may incorrectly calculate left ventricle mass measurements. If used for diagnosis, this calculation error could lead to patient misdiagnosis and incorrect treatment, potentially causing long-term health consequences.
Product
Synapse CV 6. with AR. A web-based application as the primary user interface for the processing of medical images.
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 (Drugs)·D-0332-2024·2024-02-28
Equate Cherry Cough Drops recalled for potential glass and silicone contamination
Bestco LLC is recalling Equate Cherry Cough Drops nationwide due to potential glass and silicone particulates from manufacturing deviations. Affected products are 30-drop and 160-drop bags expiring December 31, 2026.
Product
Equate Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, a) 30 drops per bag, item number 20000462, b) 160 drops per bag, item number 20000463, Bestco, 288 Mazeppa Road, Mooresville, NC 28115
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0902-2024·2024-02-28
Pizza 50/50 Flour Recalled for Potential Metal, Wood, and Foreign Material
Mennel Milling Company recalls Pizza 50/50 Unmalted flour due to potential metal, wood, gasket material, and sifter ball contamination. The affected product was distributed across KY, MI, NJ, NY, and PA.
Product
PIZZA 50/50 UNMALTED 904181 delivered as bulk product in approximately 50,000 lbs trailers
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-1142-2024·2024-02-28
Dental cement capsules recalled due to manufacturing defect affecting curing
IonoStar Plus dental cement capsules contain an incorrect plunger due to a manufacturing error. The defect prevents proper curing of the cement, making the product unsuitable for use.
Product
IonoStar Plus, Catalog (REF) Numbers: a) 2540, b)2543, c) 2544, d) 2545, e) 2546, f) 2547, g) 2549; dental cement
Category
Medical Device
Distribution
4 states
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 (Devices)·Z-1153-2024·2024-02-28
EndoVive Replacement Button Kits mislabeled with incorrect sizing
Boston Scientific is recalling EndoVive Replacement Button Kits due to sizing mislabeling that could cause undersizing and serious complications including tissue damage and sepsis.
Product
EndoVive Replacement Button Kit w/ ENFIT 28F 2.8 CM, Outer Box UPN M00509500 or M00509510.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1170-2024·2024-02-28
3M Surgical Clipper Blade Assembly Recalled Due to Burn Risk
3M recalled 764,580 Specialty Blade Assemblies for surgical clippers due to risk of burns from overheating. The blade can reach temperatures exceeding 77°C if left running improperly.
Product
3M Specialty Blade Assembly, REF 9660,70-2011-8491-1, 7100213026, used with used with 3M Surgical Clipper Catalog Number 9661L
Category
Medical Device
Distribution
0 states

How to read this listing

Filters

13901–13925 of 27735