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

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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

15401–15425 of 36683

  • SevereFDA (Drugs)·D-0356-2019·2019-01-16

    Lupin Recalls Ceftriaxone Injection Vials Due to Particulate Matter

    Lupin Pharmaceuticals is recalling Ceftriaxone for Injection USP, 500 mg, due to the presence of grey rubber particulate matter from stoppers.

    Product
    Ceftriaxone for Injection USP, 500 mg, packaged in a) one Single Use Vial (NDC 68180-622-01) and b) 10 Single Use Vials per box (NDC 68180-622-10); Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202; Manufactured by…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V019000·2019-01-16

    GM Recalls 2010-2011 Chevrolet Malibu for Air Bag Inflator Defect

    General Motors is recalling 2010-2011 Chevrolet Malibu vehicles because the driver's air bag inflator may explode during a crash, potentially causing serious injury or death.

    Product
    CHEVROLET — CHEVROLET MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0765-2019·2019-01-16

    Adam Bros. Family Farms Cauliflower Recalled for E. coli O157:H7 Contamination

    Adam Bros. Farming, Inc. is recalling specific cases of Adam Bros. Family Farms Cauliflower due to potential E. coli O157:H7 contamination. The product was distributed in 10 states.

    Product
    Adam Bros. Family Farms Cauliflower; Sold in cases with 9, 12, 16 or 20 count cases
    Category
    Food
    Distribution
    11 states
  • SevereNHTSA·19V035000·2019-01-16

    Audi Recalls A8, A7, A6, and Q7 Models for Fuel Rail Leaks

    Audi is recalling specific 2015-2018 models because fuel rails may leak, increasing the risk of fire if an ignition source is present.

    Product
    AUDI — AUDI A6, A8, A7, Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0697-2019·2019-01-16

    Swissray Medical Recalls ddRCombi Plus FP X-ray Systems Due to Lifting Column Defect

    Swissray Medical AG is recalling three ddRCombi Plus FP X-ray systems because a lifting column component may break, causing the arm to drop and potentially seriously injure patients or users.

    Product
    ddRCombi Plus FP, Model Number 8.2000.0070.0 (US Version), 8.2000.0060.0 (Europe Version) The ddRCombi Plus FP is a fully digital, multifunctional X-ray system that allows the direct digitization of X-ray information without use of cassettes or other media. It can perform all…
    Category
    Medical Device
    Distribution
    2 states
  • SevereNHTSA·19V018000·2019-01-15

    Chrysler Recalls Vehicles Due to Exploding Passenger Air Bag Inflator Risk

    Chrysler is recalling specific 2010-2016 Dodge, Chrysler, and Jeep vehicles because the passenger air bag inflator may explode during deployment, potentially causing serious injury or death.

    Product
    CHRYSLER — CHRYSLER, DODGE, JEEP 300, CHARGER, CHALLENGER, DAKOTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V015000·2019-01-14

    BMW Recalls 2000-2004 Models for Air Bag Inflator Explosion Risk

    BMW is recalling specific 2000-2004 5 Series and X5 vehicles because the air bag inflator in optional sports steering wheels may explode, posing a serious injury risk.

    Product
    BMW — BMW 540I, 525I, X5 SAV, 530I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V016000·2019-01-14

    BMW Recalls 2015 X1 Vehicles for Driver Air Bag Inflator Defect

    BMW is recalling 2015 X1 vehicles because the driver's air bag inflator may explode due to humidity, posing a risk of serious injury or death.

    Product
    BMW — BMW X1 SAV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V017000·2019-01-14

    BMW Recalls X5 and X6 Models Due to Air Bag Inflator Defect

    BMW is recalling 2007-2014 X5 and X6 models because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.

    Product
    BMW — BMW X6, X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V032000·2019-01-14

    Volvo Recalls 2018-2019 VNL Trucks for Clutch Assembly Defect

    Volvo is recalling 2018-2019 VNL trucks with automated manual transmissions because a clutch component may fail, causing unintended vehicle movement.

    Product
    VOLVO — VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V014000·2019-01-11

    Volkswagen and Audi Recall Vehicles Due to Airbag Inflator Defect

    Volkswagen is recalling specific 2015-2017 models because the driver's airbag inflator may explode during deployment, potentially causing serious injury.

    Product
    AUDI — AUDI, VOLKSWAGEN R8 SPYDER, TT ROADSTER, CC, EOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V029000·2019-01-11

    Double K Recalls 2017-2018 Hometown Trolley Buses for Brake Bolt Issue

    Double K is recalling 2017-2018 Hometown Trolley buses because loose brake caliper bolts may reduce braking effectiveness and increase crash risk.

    Product
    HOMETOWN TROLLEY — HOMETOWN TROLLEY STREETCAR, MAINSTREET, VILLAGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V030000·2019-01-11

    Double K Recalls 2017-2019 Hometown Trolley Buses for Brake Bolt Issue

    Double K is recalling 2017-2019 Hometown Trolley buses because brake caliper bolts may loosen, reducing brake effectiveness and increasing crash risk.

    Product
    HOMETOWN TROLLEY — HOMETOWN TROLLEY STREETCAR, VILLAGER, MAINSTREET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·19V008000·2019-01-09

    Subaru Recalls Vehicles Due to Passenger Air Bag Inflator Explosion Risk

    Subaru is recalling specific 2010-2014 models because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.

    Product
    SUBARU — SUBARU OUTBACK, FORESTER, LEGACY, IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·19V010000·2019-01-09

    Mercedes-Benz Recalls Vehicles Due to Passenger Air Bag Inflator Defect

    Mercedes-Benz is recalling specific 2010-2017 models because passenger air bag inflators may explode due to humidity, posing a risk of serious injury or death.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ C300, E350, GLK350, C350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0552-2019·2019-01-09

    Medtronic StealthStation Cranial Software Recall for Biopsy Depth Gauge Error

    Medtronic is recalling StealthStation Cranial and Synergy Cranial software due to an incorrect display of the Biopsy Depth Gauge that resulted in the biopsy of healthy tissue.

    Product
    StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation Cranial Optical Pocket Guide - Instructions for cranial procedures using optical localization StealthStation Cranial version 3.0, 3.1 CE 0344 Rx Only 2018-02 9735489 Revision 3 Medtronic Navigation, Inc.…
    Category
    Medical Device
    Distribution
    51 states