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.

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

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All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

25076–25100 of 26084

  • HighFDA (Devices)·Z-2160-2021·2021-08-04

    OEC 3D Imaging X-Ray Systems Recalled for Coin Cell Battery Depletion

    GE OEC Medical Systems is recalling certain OEC 3D Imaging fluoroscopic X-ray systems due to potential premature depletion of the coin cell battery used to monitor X-ray tube temperature, which could cause the system to become inoperable.

    Product
    OEC 3D Imaging, Image-Intensified Fluoroscopic X-Ray System, Mobile - Product Usage: designed to provide fluoroscopic and digital spot images of adult and pediatric populations during diagnostic, interventional, and surgical procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2162-2021·2021-08-04

    Coaxial Interventional Needles Recalled for Potential Sterilization Defects

    INNOVATIVE TOMOGRAPHY PRODUCT GMBH is recalling Coaxial Interventional Needles distributed in California due to potential sterilization defects. Needles labeled as sterile may not have been adequately sterilized, creating infection risks.

    Product
    Coaxial Interventional Needle, ITP innotom.com, CE 0297, STERILE EO for the following article numbers: Article no. KIM 22/05, Length 50 mm, diameter 22G/0,7 mm; Article no. KIM 22/07,Length 75 mm, diameter 22 G (0.7 mm); Article no. KIM 22/10, Length 100 mm, diameter 22 G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2147-2021·2021-08-04

    CooperVision CLARITI Contact Lenses Recalled for Misaligned Axis Marks

    CooperVision is recalling CLARITI 1 DAY TORIC contact lenses (Lot U0108940) because misaligned axis marks can cause blurred vision in patients.

    Product
    CLARITI 1 DAY TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2145-2021·2021-08-04

    Contact lens recall due to misaligned axis marking

    CooperVision Inc. is recalling FRESH DAY 1 DAY TORIC contact lenses (Lot R0121629) due to misaligned axis marks that may cause blurred vision in wearers.

    Product
    FRESH DAY 1 DAY TORIC Power -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0796-2021·2021-08-04

    Dole Fresh Picked Blueberries Recalled for Cyclospora Contamination

    Dole Fresh Picked Blueberries are being recalled after the Canadian Food Inspection Agency detected Cyclospora cayetanensis in the product. The recall affects multiple package sizes distributed across several U.S. states and Canadian provinces.

    Product
    Dole Fresh Picked-Emballes frais Blueberries/Bleuets: Packed in clear plastic container in the following sizes; 18 oz. - UPC: 0 71430 01154 6; Pint (16 oz.): UPC: 0 71430 01151 5; 6 oz. UPC: 07143001150 8; 24 oz. UPC: 071430011155 3 Distributed by Dole Berry Co, Winterha
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-2137-2021·2021-08-04

    Infusomat Space Pump Administration Set Recalled for Inverted Anti-Free Flow Clip

    B. Braun Medical is recalling the Infusomat Space Volumetric Pump Administration Set due to a defect where the anti-free flow clip may be inverted, potentially causing unintended medication flow. No injuries have been reported.

    Product
    Infusomat Space Volumetric Pump Administration Set, Product Code 490100
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-2143-2021·2021-08-04

    Contact Lens Recall: Misaligned Axis Mark May Cause Blurred Vision

    CooperVision is recalling CLARITI 1 DAY TORIC contact lenses with misaligned axis marks that may cause blurred vision. The defective lenses were distributed worldwide including multiple U.S. states.

    Product
    CLARITI 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2136-2021·2021-08-04

    Medtronic Endurant IIs stent graft system marker detachment recall

    Medtronic is recalling 21 Endurant IIs stent graft systems due to radiopaque marker bond detachment during device deployment. The defect could affect surgical visualization and device positioning.

    Product
    Medtronic Endurant IIs Stent Graft System Medtronic Endurant IIs Stent Graft System REF ESBF3614C103EE and ESBF3214C103E. Used to treat infrarenal abdominal aortic or aortoiliac aneurysms using an endovascular approach.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-2148-2021·2021-08-04

    Contact Lens Recall: Misaligned Axis Mark May Cause Blurred Vision

    CooperVision is recalling SPECSAVERS UMERE TORIC daily disposable contact lenses with UV blocker due to a manufacturing defect in which misaligned axis marks may cause blurred vision.

    Product
    SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V607000·2021-08-04

    2021 Volkswagen ID.4 rear seat belt assemblies may not secure child restraints

    Certain 2021 Volkswagen ID.4 vehicles have rear seat belt assemblies without proper automatic locking function, preventing child restraint systems from securing correctly. Dealers will inspect and replace affected assemblies at no cost.

    Product
    VOLKSWAGEN — 2021 VOLKSWAGEN ID.4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0818-2021·2021-08-04

    f'real Made to Order Shake Base Recalled for Undeclared Milk

    Rich Products Corp is recalling f'real Made to Order Shake Base because the outer label incorrectly identifies the product as "Smoothie Base," failing to disclose the presence of milk. Consumers with milk allergies or sensitivities face a potential health risk.

    Product
    f'real Made to Order Shake Base - 8 fl oz (237ml) cups Out packaging may read 'Smoothie-base' Lid may read ' Shake-base' 12 individual cups packed into a shrink-wrapped pulp tray
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-2159-2021·2021-08-04

    Medtronic Vectris SureScan MRI lead kits recalled for incorrect labeling

    Medtronic Neuromodulation is recalling 1131 units of Vectris SureScan MRI lead kits with incorrect electrode spacing information on packaging labels. This could affect proper device installation.

    Product
    Medtronic Vectris SureScan MRI, Catalog Numbers: a) 977A260 b) 977A275 c) 977A290
    Category
    Medical Device
    Distribution
    0 states
  • HighCPSC·21174·2021-08-04

    Two Million Dehumidifiers Recalled for Fire and Burn Hazards

    About 2 million dehumidifiers manufactured by New Widetech under multiple brand names are recalled because they can overheat and catch fire, posing fire and burn hazards. Consumers should stop using them immediately.

    Product
    Dehumidifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2154-2021·2021-08-04

    Daily Toric Contact Lenses Recalled for Misaligned Axis Mark

    CooperVision is recalling SOFMED BREATHABLES 1 DAY TORIC contact lenses (Lot W0106167) due to misaligned axis marks that can cause blurred vision. Affected lenses were distributed in the US and internationally.

    Product
    SOFMED BREATHABLES 1 DAY TORIC Power-07.00 -1.75/ 170 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2139-2021·2021-08-04

    GE CARESCAPE PDM monitor SpO2 display freezes during extended use

    GE Healthcare's CARESCAPE PDM-Masimo SpO2 physiological monitor displays can freeze after extended use without power down, preventing real-time oxygen saturation monitoring.

    Product
    CARESCAPE PDM-Masimo SpO2. Physiological data monitor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0797-2021·2021-08-04

    Amy's Tortilla Casserole Bowls Recalled for Rubber Gasket Pieces

    Amy's Kitchen is recalling Amy's Bowls Tortilla Casserole & Black Beans due to the potential presence of rubber gasket pieces from production equipment. Consumers should not eat the product and should dispose of it or return it to the store.

    Product
    Amy's Bowls, Tortilla Casserole & Black Beans; Made with organic tomatoes & Black Beans. NET WT 9.5 oz. (269g); gluten Free - Perishable - keep frozen; UPC: 0 42272 00168 2 (individual box) Case UPC: 1-00-42272-00168-9 Microwave or regular oven. In trays with plastic overlay, in
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-2164-2021·2021-08-04

    Semi-automatic Biopsy Needles Recalled Due to Sterilization Defect

    INNOVATIVE TOMOGRAPHY PRODUCT GMBH is recalling semi-automatic biopsy needles because labeled sterile units may not have been adequately sterilized. Affected devices distributed in California should not be used.

    Product
    Semi-automatic Biopsy-Needle, ITP innotom.com, CE 0297, STERILE EO for the following article numbers: Article no. BIM 18/10, Length 100 mm, Diameter 18 G (1.25 mm); Article no. BIM 18/15, Length 150 mm, Diameter 18 G (1.25 mm); Article no. BIM 18/20, Length 200 mm, Diameter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2141-2021·2021-08-04

    OxyMask O2 Adult oxygen tubing disconnect hazard recalled

    Southmedic recalled OxyMask O2 Adult oxygen masks (Model OM-1125-14, Lot W73887) due to potential oxygen tubing disconnection that could interrupt oxygen delivery.

    Product
    OxyMask O2 Adult REF OM-1125-14
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-2135-2021·2021-08-04

    Medtronic Endurant II Stent Graft Marker Detachment During Deployment

    Medtronic recalls Endurant II stent graft systems: the radiopaque marker bond may detach during deployment. The recall affects 18 devices in U.S. and international distribution. No illnesses or injuries reported.

    Product
    Endurant II/Endurant IIs Stent Graft System: Medtronic Endurant II Stent Graft System REF ETUF3214C102EE, ETCF3636C49EE, ETBF3216C166EE, and ETUF3614C102E. Used to treat infrarenal abdominal aortic or aortoiliac aneurysms using an endovascular approach.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-2134-2021·2021-08-04

    Diagnostic Genetic Probe Recalled for Unexpected Chromosome Signals

    Cytocell Ltd. is recalling CytoCell DiGeorge/VCFS genetic probes that may display unexpected chromosome signals, potentially causing misdiagnosis. Affected reagents were distributed to laboratories in multiple US states and Canada.

    Product
    CytoCell DiGeorge/VCFS TUPLE1 Region and 22q13.3 Region Probe, Model Number LPU004-A. analyte specific reagent for in vitro diagnostics
    Category
    Medical Device
    Distribution
    7 states
  • SevereNHTSA·21V601000·2021-08-03

    Fuel hose leak recall in 2021-2022 Kenworth and Peterbilt trucks

    PACCAR is recalling 688 commercial trucks due to a fuel hose leak between the fuel pump and remote fuel filter head that increases fire risk. Free fuel hose replacement is being offered.

    Product
    KENWORTH — 2021 KENWORTH T280
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V596000·2021-08-02

    2022 Mitsubishi Outlander seat belt retractor defect affects child restraints

    Mitsubishi is recalling certain 2022 Outlander vehicles due to seat belt retractors that may deactivate early, preventing child restraint systems from securing properly. Owners should contact MMNA at 1-888-648-7820 for free replacement.

    Product
    MITSUBISHI — 2022 MITSUBISHI OUTLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V598000·2021-08-02

    2020 BMW X4 Engine Software Defect Disables Braking Assist

    BMW is recalling multiple 2020-2021 models, including the X4, due to engine management software that may disable braking assist. Owners should contact BMW at 1-800-525-7417 for a free software update.

    Product
    BMW — 2020 BMW X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V595000·2021-08-02

    2021 Audi E-Tron: Unsecured glove box may interfere with air bag

    Volkswagen is recalling certain 2021 Audi E-Tron vehicles because the right hinge pin for the glove box cover may not be properly secured, potentially interfering with knee air bag deployment in a crash.

    Product
    AUDI — 2021 AUDI E-TRON
    Category
    Vehicle
    Distribution
    Distributed nationwide