The Recall Desk

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.

Filters

Agency

Category

Minimum severity

Clear filters

13926–13950 of 27735

  • 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-1152-2024·2024-02-28

    Philips Azurion X-ray Systems Disk Bay May Fail and Prevent Imaging

    The disk bay component in certain Philips Azurion x-ray systems may fail, potentially preventing diagnostic imaging and delaying procedures. Affected units have been distributed worldwide.

    Product
    Philips Azurion Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of the affected system. Affected PCs: XRay PC, Suite PC, and FlexViewing PC Azurion Model Name - Model Number: Azurion 3 M12 722063 722221; Azurion 3 M15 722064
    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-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 (Devices)·Z-1175-2024·2024-02-28

    Automated Impella Controller Software Update Resolves Pump Recognition Issue

    Abiomed is releasing software Version 8.5 for the Automated Impella Controller to fix an issue in versions 8.4 and 8.4.1 where the device failed to recognize the pump. Approximately 4,463 units were distributed nationwide.

    Product
    Automated Impella Controller (AIC), Product No. 0042-0000-US, 0042-0010-US, 0042-0040-US. Used with Impella Ventricular Support Systems (cardiovascular)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0342-2024·2024-02-28

    Adrenalin Epinephrine Injection Recalled Due to Incorrect Expiration Date Label

    Henry Schein Inc. and Glove Club HSI Gloves Inc. are recalling 1,099 vials of Adrenalin (Epinephrine) Injection because the expiration date on the repack pouch label is incorrect. The product was distributed nationwide.

    Product
    ADRENALIN — ADRENALIN (EPINEPHRINE)
    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 (Food)·F-0880-2024·2024-02-28

    Flour recalled for potential metal and foreign material contamination

    Mennel Milling Company is recalling flour products due to potential contamination with metal, wood, gasket material, and sifter balls. Affected product was distributed in Kentucky, Michigan, New Jersey, New York, Ohio, and Pennsylvania.

    Product
    160919 FLR BLE WINTER 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 (Food)·F-0879-2024·2024-02-28

    Flour Recalled for Potential Foreign Material Contamination

    Mennel Milling Company is recalling approximately 2.6 million pounds of ALL PURPOSE EN EZ BL flour due to potential contamination with metal, wood, gasket material, and sifter balls.

    Product
    15953 ALL PURPOSE EN EZ BL delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0899-2024·2024-02-28

    Mennel Milling I-52 Patent Flour Recalled for Foreign Material Contamination

    Mennel Milling Company recalled I-52 Patent Flour containing potential foreign material including metal, wood, gasket material, and sifter balls. The flour was distributed in bulk trailers across six states.

    Product
    I-52 PATENT FLOUR delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1176-2024·2024-02-28

    Philips Azurion 3 Surgical Imaging System Recalled for Power Failure Risk

    Philips is recalling 14 units of its Azurion 3 surgical imaging system due to a potential short circuit in the power inverter. The defect could cause the device to lose power and fail during surgical procedures.

    Product
    Azurion 3 with a Certeray generator -To perform image guidance in diagnostic, interventional, and minimally invasive surgery procedures Models: (1) 722221 (2) 722222 (3) 722280
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0895-2024·2024-02-28

    FDA Recalls Bulk Milling Product for Potential Foreign Material

    Mennel Milling Company is recalling its milling product (2-15969-0000) due to potential contamination with metal, wood, gasket material, and sifter balls. The product was distributed across Kentucky, Michigan, New Jersey, New York, Ohio, and Pennsylvania.

    Product
    2-15969-0000 delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1156-2024·2024-02-28

    Philips Allura Xper X-ray System Memory Modules May Stop Functioning

    Philips Allura Xper fluoroscopic X-ray systems may experience memory module failures that cause the system to stop functioning and prevent imaging. This malfunction could delay critical medical procedures.

    Product
    Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the DIMMs (Dual In-line Memory Modules) used with affected systems. Allura Xper Model Name - Model Number: Allura Xper FD10 722003 722010 722026; Allura Xper FD10/10 722005 722011 722027;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0337-2024·2024-02-28

    Voriconazole Oral Suspension Recalled for Missing Package Insert

    Lupin Pharmaceuticals recalls Voriconazole for Oral Suspension (40mg/mL) due to missing or incorrect package inserts on affected batches distributed in Ohio, Illinois, and New Jersey.

    Product
    VORICONAZOLE — VORICONAZOLE (VORICONAZOLE)
    Category
    Drug
    Distribution
    3 states
  • HighFDA (Food)·F-0887-2024·2024-02-28

    Pizza 50/50 Unmalted Flour Recalled for Potential Foreign Material

    Mennel Milling Company is recalling approximately 2.6 million pounds of PIZZA 50/50 UNMALTED flour due to potential contamination with metal, wood, gasket material, and sifter balls.

    Product
    PIZZA 50/50 UNMALTED delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • 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
  • 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
  • HighCPSC·24740·2024-02-22

    Polaris MATRYX Snowmobiles Recalled for Primary Clutch Failure Hazard

    Polaris is recalling Model Year 2022–2024 MATRYX snowmobiles with PATRIOT 650 and 850 engines because the primary clutch can fail and separate from the vehicle, creating an injury hazard. Polaris has received 109 reports of clutch failure, including one incident resulting in a laceration injury.

    Product
    Model Year 2022-2024 MATRYX Snowmobiles equipped with PATRIOT 650 and 850 Engines
    Category
    Vehicle
    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·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
  • 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·24126·2024-02-22

    Cascade Designs MSR Camping Cooking Pots Recalled for Burn and Scald Hazards

    Cascade Designs is recalling select MSR camping cooking pots because the handle can detach or become loose, spilling hot food and liquids and causing burn or scald injuries. The company has received 22 reports of handle problems, including two burn injuries.

    Product
    MSR camping cooking pots
    Category
    Consumer Product
    Distribution
    Distributed nationwide