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.

Filters

Agency

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

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

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

Clear filters

11201–11225 of 36635

  • SevereFDA (Food)·F-0972-2020·2020-06-10

    K F K Seasonings Recalls Azure Market Chili Powder for Undeclared Allergens

    K F K Seasonings LLC is recalling 96 lbs of Azure Market Chili Powder, Mild, Organic due to undeclared tree nuts and Crustacea.

    Product
    Chili Powder, Mild, Organic is a blend, Item # 90030. Packaged in 1 lb. bags and sold under brand Azure Market. This product contains "Organic Chili Peppers, Salt, Organic Spices, Organic Garlic, Organic Sunflower Oil". The Azure Market label listed the lot # 90030041520 and…
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2257-2020·2020-06-10

    Siemens ARTIS icono X-Ray Systems Recalled for Incorrect Vessel Quantification

    Siemens is recalling five ARTIS icono X-ray systems because software may fail to detect vessels or provide incorrect measurements, potentially leading to wrong diagnoses.

    Product
    ARTIS icono systems with Quantification Application SW (QVA/QCA) on a standalone XWP computer, an interventional Fluoroscopic X-Ray System Model Number: 11327600
    Category
    Medical Device
    Distribution
    4 states
  • SevereFDA (Devices)·Z-2165-2020·2020-06-10

    Insulet Recalls Omnipod DASH Insulin Systems Due to Bolus Calculation Error

    Insulet Corporation is recalling 1,773 Omnipod DASH Insulin Management Systems (mmol/L configuration) because the Bolus Calculator may fail to accurately subtract insulin on board after two months of use.

    Product
    Omnipod DASH Insulin Management System (mmol/L configuration), Catalog Number PT000011 M/D: INT1D001MM - Product Usage: is intended for subcutaneous delivery of insulin at set and variable rates for the management of diabetes mellitus in persons requiring insulin.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2254-2020·2020-06-10

    Multifire Endo Hernia Stapler Recalled for Manufacturing Assembly Error

    Covidien is recalling Multifire Endo Hernia Staplers due to a manufacturing error that may cause staples to fail to advance properly during use.

    Product
    Multifire Endo Hernia 0 12mm Stapler with 4.8mm Disposable Loading Unit , Part No. 174025 - Product Usage: has application in endoscopic general surgery procedures for fixation of mesh in the repair of hernial defects and in other surgical specialties for approximation of…
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2174-2020·2020-06-10

    FDA Recalls Sterile Surgical Packs Due to Unregistered Facility

    American Contract Systems is recalling 2,868 sterile surgical packs because they were manufactured in a facility not registered by the FDA.

    Product
    Sterile Custom Packs to be used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V341000·2020-06-10

    KME Fire Trucks Recalled for Potential Braking Mechanism Separation

    KME is recalling specific fire trucks because the optional Telma induction braking mechanism may separate from the vehicle while moving, increasing crash risk.

    Product
    KME — KME PREDATOR PANTHER, PREDATOR SS, PREDATOR, COMMERCIALCAB/ CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2231-2020·2020-06-10

    Zimmer Biomet Recalls Vital MIS Spinal Fixation Implants Due to Locking Issues

    Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because the extended tab screws may not lock adequately, causing the closure top to back out after surgery.

    Product
    Vital MIS Spinal Fixation system implants CANN BL POLY EXT 8.5X55MM, Item Number 811M8555 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0973-2020·2020-06-10

    K F K Seasonings Recalls Organic Chipotle Chile Ground for Undeclared Tree Nuts

    K F K Seasonings is recalling 230 lbs of Organic Chipotle Chile Ground sold as Blue Chip in Oregon and Utah due to undeclared tree nuts.

    Product
    Organic Chipotle Chile Ground, Item # 90033. Packaged in 40 lbs. box and sold under brand Blue Chip. This product contains Chipotle Chile pepper. The Blue Chip label listed the lot # 032918. No UPC. Product distributed by Blue Chip Corp. UT.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2228-2020·2020-06-10

    Zimmer Biomet Recalls Vital MIS Spinal Fixation Implants Due to Locking Issues

    Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because reports indicate the extended tab screws may not lock adequately, causing the closure top to back out after surgery.

    Product
    Vital MIS Spinal Fixation system implants CANN BL POLY EXT 8.5X40MM, Item Number 811M8540 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2211-2020·2020-06-10

    Zimmer Biomet Recalls Vital MIS Spinal Fixation Implants Due to Locking Issues

    Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because reports indicate the extended tab screws may not lock adequately, causing the closure top to back out after surgery.

    Product
    Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 4.5X35MM, Item Number 810M4535 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2229-2020·2020-06-10

    FDA Recalls Zimmer Biomet Vital MIS Spinal Fixation Implants

    Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants due to reports of inadequate locking of extended tab screws and post-operative backing out of the closure top.

    Product
    Vital MIS Spinal Fixation system implants CANN BL POLY EXT 8.5X45MM, Item Number 811M8545 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2255-2020·2020-06-10

    FDA Recalls Multifire Endo Hernia Staplers Due to Assembly Error

    The FDA is recalling 12,610 Multifire Endo Hernia Staplers due to a manufacturing error that may cause staples to fail to advance properly.

    Product
    Multifire Endo Hernia 0 12mm Stapler with 4.0mm Disposable Loading Unit , Part No. 174027 - Product Usage: has application in endoscopic general surgery procedures for fixation of mesh in the repair of hernial defects and in other surgical specialties for approximation of…
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2217-2020·2020-06-10

    Zimmer Biomet Recalls Vital MIS Spinal Fixation Implants Due to Locking Failure

    Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because reports indicate the closure top may back out of the screw post-operatively.

    Product
    Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 5.5X50MM, Item Number 810M5550 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2207-2020·2020-06-10

    Nobel Biocare Recalls Dental Implants Due to Incorrect Length Labeling

    Nobel Biocare is recalling 221 dental implants because the label may incorrectly state the length as 11.5mm instead of the actual 15mm, posing a risk of nerve damage.

    Product
    NobelActive Internal NP 3.5x15mm Endosseus dental implant, REF: 34128, Rx Only, Sterile R, CE, UDI: (01)07332747010619
    Category
    Medical Device
    Distribution
    28 states
  • SevereFDA (Devices)·Z-2233-2020·2020-06-10

    Zimmer Biomet Recalls Vital MIS Spinal Fixation Implants Due to Locking Issues

    Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because reports indicate the extended tab screws may not lock adequately, causing the closure top to back out after surgery.

    Product
    Vital MIS Spinal Fixation system implants VITAL MIS TAB BREAKER, Item Number 850M0055 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is indicated…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V340000·2020-06-09

    Mercedes-Benz Metris Recall for Driveshaft Attachment Defect

    Daimler Vans USA is recalling 2019 Mercedes-Benz Metris vans because the driveshaft may not be attached correctly, risking loss of drive or unexpected airbag deployment.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V337000·2020-06-09

    Jayco Recalls 2020 Motorized RVs Due to Window Glass Detachment Risk

    Jayco is recalling 2020 motorized recreational vehicles because the adhesive on frameless windows may fail, allowing glass to detach and become a projectile.

    Product
    JAYCO — JAYCO, ENTEGRA REDHAWK, QWEST, SENECA, EMBLEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V335000·2020-06-09

    ARBOC Spirit of America and Liberty Buses Recalled for Fire Risk

    ARBOC is recalling 113 Spirit of America and Spirit of Liberty buses because misrouted power cables may short circuit, increasing the risk of a fire.

    Product
    ARBOC — ARBOC SPIRIT OF AMERICA, SPIRIT OF LIBERTY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V334000·2020-06-09

    Chrysler Recalls 2017-2020 Pacifica Plug-in Hybrids for Fire Risk

    Chrysler is recalling 2017-2020 Pacifica Plug-in Hybrids because a high-resistance electrical connection may overheat and cause a fire.

    Product
    CHRYSLER — CHRYSLER PACIFICA PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V331000·2020-06-08

    Ford Recalls Vehicles Due to Door Latch Repair Defects

    Ford is recalling specific 2011-2016 vehicles because previous door latch repairs may have been incomplete, potentially allowing doors to open while driving.

    Product
    FORD — FORD, LINCOLN C-MAX, FIESTA, FOCUS, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V329000·2020-06-05

    Mercedes-Benz Recalls 2020 GLE and GLS Models for Suspension Defect

    Mercedes-Benz is recalling 2020 GLE 450, GLS 450, and GLS 580 4MATIC vehicles because leaking suspension components may affect handling and increase crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 450, GLS 450, GLS 580 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V328000·2020-06-05

    Mercedes-Benz Recalls 2020 Models for Rear Seatback Latch Defect

    Mercedes-Benz is recalling 2020 E450, GLC300, and AMG models because the left-rear seatback latch may fail, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 450, GLC 300, AMG E63S, AMG GLC63
    Category
    Vehicle
    Distribution
    Distributed nationwide