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

23251–23275 of 39702

  • SevereFDA (Devices)·Z-2694-2016·2016-09-14

    MicroPort Recalls Advance II Modular Tibial Bases Due to Component Loosening

    MicroPort Orthopedics is recalling Advance II Modular Tibial Bases because of a higher-than-expected revision rate caused by component loosening.

    Product
    ADVANCE(R) II MODULAR TIBIAL BASE W/SCREWHOLES, Knee Tibial Base, REF KTTIHA11, SIZE 1+; SURFACE POROUS, HA COATED; FIT CEMENTLESS; USE W/ SIZE 1 FEMUR & SIZE 1 TIBIAL INSERT; CONTENTS, 1 EACH, STERILE R, Rx ONLY, MicroPort Knee Systems Total Knee Systems MicroPort Total Knee…
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2699-2016·2016-09-14

    MicroPort Recalls Advance II Modular Tibial Base Components

    MicroPort Orthopedics is recalling Advance II Modular Tibial Base components due to a higher than expected revision rate caused by component loosening.

    Product
    ADVANCE(R) II MODULAR TIBIAL BASE W/SCREWHOLES, Knee Tibial Base, REF KTTIHA40, SIZE 4 STD; SURFACE POROUS, HA COATED; FIT CEMENTLESS; USE W/ SIZE 4 FEMUR & SIZE 4 TIBIAL INSERT; CONTENTS, 1 EACH, STERILE R, Rx ONLY, MicroPort Knee Systems Total Knee Systems MicroPort Total…
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·16V662000·2016-09-14

    Gillig Recalls 2014-2016 Low Floor Buses Due to Brake Hose Fraying

    Gillig is recalling 2014-2016 Low Floor transit buses because rear brake hoses can fray, potentially causing brake lockup or failure and increasing crash risk.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2697-2016·2016-09-14

    MicroPort Advance II Modular Tibial Base Recalled for Component Loosening

    MicroPort Orthopedics is recalling Advance II Modular Tibial Bases due to a higher than expected revision rate caused by component loosening.

    Product
    ADVANCE(R) II MODULAR TIBIAL BASE W/SCREWHOLES, Knee Tibial Base, REF KTTIHA30, SIZE 3 STD; SURFACE POROUS, HA COATED; FIT CEMENTLESS; USE W/ SIZE 3 FEMUR & SIZE 3 TIBIAL INSERT; CONTENTS, 1 EACH, STERILE R, Rx ONLY, MicroPort Knee Systems Total Knee Systems MicroPort Total…
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2768-2016·2016-09-14

    Bayer Certegra Workstation Recalled for Fire and Smoke Risk

    Bayer Healthcare is recalling 165 Certegra Workstations used with Medrad Stellant CT Injection Systems because they may produce smoke and sparks of fire.

    Product
    Certegra Workstation used in conjunction with Medrad Stellant CT Injection System Catalog Number # CWKS DISPLAY Serial Numbers The Medrad Stellant CT Injector System is intended for the specific purpose of injecting intravenous contrast media into humans for diagnostic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1586-2016·2016-09-14

    Schnucks Recalls Maytag Blue Cheese Due to Listeria Risk

    Schnucks Markets is recalling Maytag Blue cheese cut and wrapped in-store due to potential Listeria monocytogenes contamination. The product was sold in Missouri, Illinois, and Iowa.

    Product
    Maytag Blue cheese cut and wrapped in clear plastic wrap at store level, sold in various sizes (approximately 3-4 oz pieces), labeled with company issued Maytag Blue cheese label and Schnuck Markets scale label, UPC 0021806200000.
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·16V658000·2016-09-13

    Freightliner Trucks Recalled for Brake Caliper Bolt Torque Issues

    Daimler Trucks North America is recalling 2016-2017 Freightliner M2 and 114 SD trucks because brake caliper mounting bolts may be incorrectly torqued, potentially reducing braking ability.

    Product
    FREIGHTLINER — FREIGHTLINER 114SD, BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E071000·2016-09-13

    EVS Emergency Vehicle Seats Recalled for Slide Track Defect

    EVS is recalling emergency vehicle seats with Dometic/Atwood slide tracks that may not engage properly, increasing injury risk in a crash.

    Product
    SEATS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V654000·2016-09-12

    FCCC Motorhome Chassis Recall for Brake Signal Defect

    Daimler Trucks is recalling 2013-2016 FCCC XCM, XCR, and XCL motorhome chassis because a brake signal may remain active, causing towed device brakes to drag and potentially overheat.

    Product
    FCCC — FCCC XCL, XCR, XCM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·079-2016·2016-09-10

    MIH Marketing Recalls Meat and Poultry Products Due to Insanitary Conditions

    MIH Marketing and Sales is recalling approximately 662,049 pounds of raw chicken products stored under insanitary conditions, including rodent activity.

    Product
    MIH Marketing and Sales Recalls Meat and Poultry Products Due To Insanitary Conditions
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·078-2016·2016-09-09

    PT Farm Recalls Lamb Products Due To Possible E. Coli Contamination

    PT Farm, LLC is recalling approximately 15 pounds of raw lamb products sold in Massachusetts due to possible E. coli contamination.

    Product
    Montshire Packing, LLC — PT Farm, LLC Recalls Lamb Products Due To Possible E. Coli Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·16V653000·2016-09-09

    BMW Recalls M2, M3, and M4 Models for Rear Sub-Frame Bolt Issue

    BMW is recalling specific M2, M3, and M4 vehicles because reused rear sub-frame bolts may loosen, affecting handling and increasing crash risk.

    Product
    BMW — BMW M3, M4, M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·077-2016·2016-09-08

    Carnival Supermarket Recalls Ground Beef Due To E. Coli O157:H7

    Carnival Supermarket in Chula Vista, California, is recalling approximately 35 pounds of ground beef sold on Sept. 1, 2016, due to possible E. coli O157:H7 contamination.

    Product
    Paradise Valley Market, Inc. (Carnival Supermarket) Recalls Ground Beef Productsdue To Possible E. Coli O157:H7 Adulteration
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V652000·2016-09-08

    Cambli Recalls 2014-2015 Beverage Industry Trailers Due to Brake Defect

    Cambli is recalling 2014-2015 Beverage Industry trailers because improperly machined spring brake valves may delay braking, causing the trailer to roll away.

    Product
    CAMBLI — CAMBLI BEVERAGE INDUSTRY TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V648000·2016-09-08

    Audi Recalls 2017 Q7 Vehicles Due to Electric Power Steering Defect

    Volkswagen Group of America is recalling 2017 Audi Q7 vehicles because the electric power steering control unit may short circuit, causing a loss of steering assist and increasing crash risk.

    Product
    AUDI — AUDI Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1999-2016·2016-09-07

    General Mills Recalls Nature Valley Bars Due to Listeria Risk

    General Mills is voluntarily recalling Nature Valley Simple Nut Bars and Protein Chewy Bars due to potential Listeria monocytogenes contamination from sunflower kernels.

    Product
    Nature Valley Simple Nut Bars, Almond, Cashew & Sea Salt, Carton UPC 000-16000-46474, Case UPC 100-16000-46474, 4 bars/carton, 4 1.17 OZ (33 g) BARS, NET WT 4.68 OZ (132 g). Nature Valley Simple Nut Bars, Almond, Cashew & Sea Salt, Carton UPC 000-16000-41301, Case UPC…
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-2028-2016·2016-09-07

    Let's Do Lunch Recalls Beef Sausage & Cheese Mini Bagel Sandwiches

    Let's Do Lunch, Inc. is recalling Beef Sausage & Cheese Mini Bagel Sandwiches due to potential Listeria monocytogenes contamination. The product was distributed in nine U.S. states.

    Product
    Beef Sausage & Cheese Mini Bagel Sandwich Product ID C80916
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-2033-2016·2016-09-07

    Let's Do Lunch Recalls All American Burger for Listeria Risk

    Let's Do Lunch, Inc. is recalling 590 cases of All American Burger due to potential Listeria monocytogenes contamination.

    Product
    All American Burger Product ID 470007, C47007
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-2026-2016·2016-09-07

    Let's Do Lunch Recalls Cheeseburger Sliders for Listeria Risk

    Let's Do Lunch, Inc. is recalling 2,085 cases of Cheeseburger Sliders due to potential Listeria monocytogenes contamination. The product was distributed to nine U.S. states.

    Product
    Cheeseburger Sliders Product ID C47220, 470220
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-2022-2016·2016-09-07

    Awrey's Bakery Recalls Deep Chocolate Sheet Cakes for Undeclared Walnuts

    Minnie Marie Bakers, Inc. dba Awrey's Bakery is recalling Deep Chocolate Sheet Cakes in Ohio due to undeclared walnuts, posing a risk to those with tree nut allergies.

    Product
    Deep Chocolate Sheet Cake 8x12 28.125 lb case 20, 22.5 oz cakes per case
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-2009-2016·2016-09-07

    Raw Pistachios Recalled Due to Potential Salmonella Contamination

    International Foodsource LLC is recalling raw shelled pistachios due to potential Salmonella contamination found in FDA testing.

    Product
    IFS Web Bulk Pistachio Raw Shelled 80% Wholes Net Wt. 30 lb. (13 kg) International Foodsource LLC 52 Richboynton Rd. Dover NJ 07801 UPC 790429239630
    Category
    Food
    Distribution
    Distributed nationwide