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 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.

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14501–14525 of 89769

  • HighFDA (Devices)·Z-1085-2024·2024-02-21

    Stryker Trevo Trak 21 Microcatheter Recalled for Unevaluated Intended Use

    Stryker, Inc. is recalling 63 units of the Trevo Trak 21 Microcatheter because the device instructions contain an intended use that has not been evaluated by the FDA.

    Product
    Stryker Neurovascular, Trevo Trak 21 Microcatheter, REF 90338, 0.021in X162cm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0871-2024·2024-02-21

    Dannon Plain Yogurt 32oz cartons recalled for potential sanitizer contamination

    DANONE US LLC is recalling Dannon Plain Yogurt 32oz cartons distributed in Georgia due to potential contamination with sanitizer. The affected product expires 03/13/24.

    Product
    Dannon Plain Yogurt packaged in 32oz plastic carton with lid - 6 cartons per case
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1078-2024·2024-02-21

    Skin Graft Carrier Recalled for Manufacturing Ratio Defect

    Zimmer Surgical Inc. is recalling 3:1 Dermacarrier skin graft carriers due to a manufacturing defect where the ridge pattern is 1.5:1 instead of 3:1, potentially causing tissue damage or additional grafting.

    Product
    3:1 Dermacarrier, Model Number 00219501300, skin graft carrier
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1073-2024·2024-02-21

    Philips Recalls ProxiDiagnost Radiography Systems for Patient Data Display and Security Issues

    Philips is recalling 20 ProxiDiagnost radiography/fluoroscopy systems due to two issues: potential display of previous patient images when scanning new patients, and a security vulnerability allowing unauthorized data access. No injuries have been reported.

    Product
    ProxiDiagnost upgrade- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref:706150
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1066-2024·2024-02-21

    Bone Filler Tubes Recalled Due to Manufacturing Process Defect

    The FDA is recalling 89 AFT Bone Filler Tubes due to a manufacturing process defect that could cause extrudability issues during surgery. The filling process did not demonstrate adequate capability.

    Product
    AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler)
    Category
    Medical Device
    Distribution
    1 state
  • HighNHTSA·24V126000·2024-02-21

    Spencer Recalls 2020 Pumper Fire Trucks Due to Electrical Fire Risk

    Spencer is recalling 2020 Pumper fire trucks because a firmware defect in Weldon nodes may cause overloaded electrical circuits, increasing the risk of fire.

    Product
    SPENCER — SPENCER PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1072-2024·2024-02-21

    Philips ProxiDiagnost N90 X-ray System Recall for Patient Data and Security Issues

    Philips is recalling 138 U.S. units of its ProxiDiagnost N90 radiography system due to two identified issues. The system may display incorrect patient images during scan transitions, and a security vulnerability could allow unauthorized data access with physical device access.

    Product
    ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref: (1)706100 (2)706110
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1139-2024·2024-02-21

    BIOFIRE BCID2 Blood Culture Panel Recalled for False Positive Candida tropicalis Results

    BioFire Diagnostics recalls BIOFIRE BCID2 panels due to false positive Candida tropicalis detection when used with certain BD BACTEC culture vials. The vials contain non-viable organism DNA that triggers incorrect positive results.

    Product
    BIOFIRE Blood Culture Identification 2 (BCID2) Panel when used with: BD BACTEC Lytic Anaerobic medium BD BACTEC Peds Plus medium BD BACTEC Plus Aerobic medium BD BACTEC Plus Anaerobic medium BD BACTEC Standard Aerobic medium BD BACTEC Standard Anaerobic medium The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1056-2024·2024-02-21

    Samsung GM85 Mobile X-ray System Welding Frame Defect Arm Fall Risk

    NeuroLogica is recalling 261 Samsung GM85 mobile x-ray systems due to a welding defect in the moving arm frame that could cause the arm to fall, risking bodily injury.

    Product
    Samsung Digital Diagnostic Mobile X-ray System, Model GM85.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1088-2024·2024-02-21

    Philips CombiDiagnost R90 Fluoroscopy Display May Show Previous Patient Images

    Philips CombiDiagnost R90 fluoroscopy systems may display a previous patient's images during radiography examination, potentially showing different image content, format, and size that could affect imaging accuracy.

    Product
    CombiDiagnost R90 1.1 (709031)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1077-2024·2024-02-21

    Medical Device Recall: Heart-Lung Machine Component Sterile Barrier Defect

    The BEQ-HLS 7050 USA HLS Set Advanced 7.0 is recalled due to a compromised sterile barrier on its Emergency Priming Line component. This defect may cause inflammation, sepsis, or infection.

    Product
    BEQ-HLS 7050 USA, HLS Set Advanced 7.0, Product Code/Part Number 70106.9078. Used with the CARDIOHELP heart-lung machine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V123000·2024-02-20

    Porsche 911 rear seat belts may not secure a child restraint

    Porsche is recalling certain 2023 911 vehicles over the rear three-point seat belts, where an unsecured child restraint system can increase the risk of injury in a crash.

    Product
    PORSCHE — PORSCHE 911 CARRERA, 911 CARRERA S, 911 TARGA 4S, 911 TURBO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V121000·2024-02-19

    Volvo Recalls 2024-2025 VNL and VNR Trucks for Steering Defect

    Volvo Trucks is recalling 2024-2025 VNL and VNR models because improperly heat-treated steering gear shafts may crack, risking loss of steering control.

    Product
    VOLVO — VOLVO VNL, VNR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V120000·2024-02-19

    2023–2024 Horton Ford Emergency Vehicles Brake Line Recall

    Halcore Group, Inc. is recalling certain 2023–2024 Horton emergency vehicles built on Ford F-450, F-550, and F-600 chassis because the left rear brake line can contact and be damaged by the strut mount when the rear suspension is lowered, risking brake fluid leakage and loss of brakes.

    Product
    HORTON — HORTON FORD F-450, FORD F-600, FORD F-550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V122000·2024-02-19

    2024 Mack Granite trucks recalled for insufficient air brake tank volume

    Mack Trucks is recalling certain 2022–2024 Granite vehicles because the air tanks do not have sufficient volume for the brake system, reducing braking performance and increasing crash risk.

    Product
    MACK — MACK GRANITE (GR)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V115000·2024-02-16

    Mercedes-Benz Recalls 31,848 Vehicles for Defective 80-Amp Fuses

    Mercedes-Benz is recalling 31,848 vehicles because defective 80-Amp fuses may fail, causing loss of drive power, safety functions, or fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH GLC 300, C 300, E 350, E 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V117000·2024-02-16

    Mercedes-Benz Recalls 2024 GLE Models Due to Accelerator Pedal Bracket Defect

    Mercedes-Benz is recalling 2024 GLE 350, GLE 450, and AMG GLE53 vehicles because an improperly welded accelerator pedal bracket may break or detach, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLE53 4MATIC+, GLE 350, GLE 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·007-2024·2024-02-15

    Don Novo & Son Recalls Ready-to-Eat Meat Products Due to Listeria

    Don Novo & Son is recalling approximately 9,330 pounds of ready-to-eat meat products in Florida due to possible Listeria monocytogenes contamination.

    Product
    Don Novo & Son — Don Novo & Son Recalls Ready-To-Eat Meat Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    1 state
  • HighCPSC·24118·2024-02-15

    Bell Soquel Youth Bicycle Helmets Recalled for Head Injury Risk

    Bell Sports is recalling about 2,425 Bell Soquel Youth Helmets because the strap anchor can become dislodged during a crash, reducing protection and posing a risk of head injury.

    Product
    Bell Soquel Youth Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V111000·2024-02-15

    Jeep Wrangler Defrosting System Software Error May Impair Visibility

    Chrysler is recalling affected Jeep Wrangler and Grand Cherokee models due to a software defect in the windshield defroster system that may reduce visibility. Affected owners should contact Chrysler for a free software update.

    Product
    JEEP — JEEP GRAND CHEROKEE, WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V114000·2024-02-15

    2023-2024 Honda Odyssey and 2024 Acura RDX steering defect

    Honda is recalling certain 2023-2024 Odyssey and 2024 Acura RDX vehicles due to improper steering gear box assembly tightening. Water can enter the assembly, causing corrosion and loss of steering control.

    Product
    HONDA — HONDA, ACURA ODYSSEY, RDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24117·2024-02-15

    Frigidaire Rear-Controlled Ranges Recalled for Electrical Shock and Electrocution Hazards

    Electrolux Group is recalling about 1,800 Frigidaire rear-controlled ranges because the control panel can detach from the unit, creating electrical shock and electrocution hazards. Consumers should stop using the ranges immediately and contact Electrolux for a free repair.

    Product
    Frigidaire rear-controlled ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide