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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15576–15600 of 36701

  • SevereNHTSA·18V889000·2018-12-14

    Autocar Recalls 2019 Xpeditor Vehicles Due to Loose Driveline Bolts

    Autocar is recalling 2019 Xpeditor vehicles because universal joint strap bolts may not be properly tightened, which could cause the drive shaft to detach and increase crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V888000·2018-12-13

    Toyota Recalls 2018-2019 Tacoma Vehicles Due to Brake Master Cylinder Defect

    Toyota is recalling 2018-2019 Tacoma vehicles because improper machining of the brake master cylinder may damage internal seals, potentially reducing brake performance and increasing crash risk.

    Product
    TOYOTA — TOYOTA TACOMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V887000·2018-12-13

    Toyota Recalls Land Cruiser and Lexus LX 570 for Air Bag Deactivation Risk

    Toyota is recalling 2008-2019 Land Cruiser and Lexus LX 570 vehicles because a broken wire harness may deactivate front passenger air bags, increasing injury risk in crashes.

    Product
    TOYOTA — TOYOTA, LEXUS LAND CRUISER, LX570
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E115000·2018-12-13

    Lifeworks Recalls Heated Seat Cushions and Blankets Due to Fire Risk

    Lifeworks is recalling specific Armor All heated seat cushions and blankets sold at Meijer because they may overheat and melt, posing a fire and injury risk.

    Product
    EQUIPMENT:ELECTRICAL recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V883000·2018-12-12

    Toyota, Lexus, and Pontiac Recall Vehicles Due to Air Bag Inflator Defect

    Toyota, Lexus, and Pontiac are recalling specific 2002-2007 vehicles because passenger air bag inflators may explode during deployment, posing a risk of serious injury.

    Product
    PONTIAC — PONTIAC, LEXUS, TOYOTA VIBE, SC, SEQUOIA, COROLLA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0536-2019·2018-12-12

    Zimmer Biomet Recalls Humeral Guide Wires Due to Sterility Compromise

    Zimmer Biomet is recalling 8,027 Humeral Guide Wires because creases in the sealing area may compromise product sterility.

    Product
    Zimmer Humeral Guide Wire - Ball Tip, 2.4 mm Diameter, 70 cm Length Item Number: 47-2255-008-00 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0751-2019·2018-12-12

    Green Cedar Ackawi cheese recalled due to Listeria monocytogenes contamination

    Harb Dairy is voluntarily recalling Green Cedar Ackawi cheese in Michigan after FDA and state officials confirmed the product tested positive for Listeria monocytogenes.

    Product
    Green Cedar Ackawi cheese in small clear plastic shrink wrapped packaging bearing a sell by date of March 26, 2019 or later. The sell by date is on a white sticker on the back of the product. , Keep Refrigerated
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0549-2019·2018-12-12

    Invacare Hydraulic Patient Lifts Recalled for Potential Caster Separation

    Invacare is recalling 73,703 hydraulic patient lifts because a mounting bolt may loosen, causing the caster to separate and the lift to tilt.

    Product
    Invacare 9805 and 9805P Hydraulic Patient Lifts, Model Nos. 9805 and 9805P The intended use of a Non-AC-Powered patient lift is to lift and transfer a patient from one surface to another, as from a bed to a wheelchair. The device includes straps and a sling to support the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0463-2019·2018-12-12

    GE Healthcare Recalls CARESCAPE R860 Inspiratory Safety Guards

    GE Healthcare is recalling CARESCAPE R860 Inspiratory Safety Guards because they may disconnect from the breathing circuit, potentially causing loss of ventilation and hypoxia in patients.

    Product
    GE HEALTHCARE CARESCAPE R860 Inspiratory Safety Guard, Part Numbers: a) 2066713-001 (single pack) b) 2083208-001 (box of ten singles) The CARESCAPE R860 ventilator is designed to provide mechanical ventilation or support to neonatal, pediatric, and adult patients weighing…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0544-2019·2018-12-12

    Philips Brilliance 40 CT Systems Recalled for Gantry Cover Separation Risk

    Philips is recalling 6,343 Brilliance 40 CT systems nationwide due to a potential fiberglass resin separation that could cause the gantry front cover to fall.

    Product
    Brilliance 40, Model 728235 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0717-2019·2018-12-12

    Jay Robb Unflavored Egg White Protein Recalled for Undeclared Milk

    Agropur MSI Ingredients LLC is recalling Jay Robb Unflavored Egg White Protein due to undeclared milk. The recall covers 1,956 pouches distributed nationwide.

    Product
    Jay Robb Unflavored Egg White Protein, Net Weight 24 oz (1.5lbs) 680g. Dietary Supplement. UPC 03907-00492. Jay Robb, Inc., Jupiter, FL 33458
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0533-2019·2018-12-12

    Zimmer Biomet Recalls Guide Wires Due to Sterility Compromise

    Zimmer Biomet is recalling 2,080 units of ZMS Intramedullary Fixation Smooth Guide Wires because creases in the packaging may compromise sterility.

    Product
    Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire, 2.4 mm Diameter, 100 cm Length Item Number: 47-2237-033-00 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V884000·2018-12-12

    Blue Bird Recalls School Buses Due to Brake and Fuel Line Fire Risk

    Blue Bird is recalling 2013-2020 Vision school buses because improperly routed brake lines and shifter cables may cause fluid or fuel leaks, increasing fire risk.

    Product
    BLUE BIRD — BLUE BIRD VISION, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0539-2019·2018-12-12

    Zimmer Biomet Recalls Natural Nail System Guide Wires Due to Sterility Compromise

    Zimmer Biomet is recalling 3,764 units of Natural Nail System Tear Drop Guide Wires because creases in the packaging seal may compromise sterility.

    Product
    Zimmer Natural Nail¿ System - Tear Drop Guide Wire, 2.4 mm Diameter, 100 cm Length Item Number: 47-2490-097-01 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0737-2019·2018-12-12

    Ottogi Jin Ramen Mild Recalled for Undeclared Egg Allergen

    Ottogi America Inc. is recalling Ottogi Jin Ramen Mild 5-packs due to an undeclared egg allergen. The product was distributed in five U.S. states and Canada.

    Product
    Ottogi Jin Ramen Mild NET WT. 1lb 5.16oz, 600g (120gx5) 5PK Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·18V880000·2018-12-11

    Blue Bird Recalls 2019 School Buses for Parking Brake Cable Defect

    Blue Bird is recalling 2019 All American and Vision school buses because the parking brake cable may disengage, allowing the bus to move unintentionally.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V881000·2018-12-11

    Blue Bird Recalls 2019 Transit Buses Due to Parking Brake Defect

    Blue Bird is recalling 2019 All American and Vision transit buses because the parking brake cable may disengage, allowing the bus to move unintentionally.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·120-2018·2018-12-10

    CTI Foods Recalls Pork and Poultry Sausage Due to Metal Contamination

    CTI Foods is recalling frozen Jimmy Dean sausage links that may contain metal pieces. No illnesses have been reported, but consumers should discard the product.

    Product
    CTI Foods LLC. — CTI Foods LLC, Recalls Ready-To-Eat Pork and Poultry Sausage Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·18V877000·2018-12-10

    Thomas Built Buses Recalls Saf-T-Liner C2 School Buses for Roof Adhesive Defect

    Daimler Trucks North America is recalling 2017-2019 Thomas Built Buses Saf-T-Liner C2 school buses because improperly applied roof adhesive may reduce roof header strength during a rollover crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·119-2018·2018-12-09

    3-D Meats Recalls Beef Snack Sticks for Undeclared Milk Allergen

    3-D Meats, LLC is recalling approximately 47 pounds of ready-to-eat beef snack sticks because they are misbranded and may contain undeclared milk, a known allergen.

    Product
    3-D Meats, LLC Recalls Ready-To-Eat Beef Snack Stick Products due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·18V870000·2018-12-07

    PACCAR Recalls 2018 Kenworth and Peterbilt Trucks for Seat Belt Defect

    PACCAR is recalling 2018 Kenworth and Peterbilt trucks because seat belt buckles may be glued instead of sewn, risking separation in a crash.

    Product
    KENWORTH — KENWORTH, PETERBILT T880, T680, 579, 567
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·118-2018·2018-12-07

    Amboy Group Recalls Poultry Products for Undeclared Allergens

    Amboy Group, LLC is recalling raw boneless and skinless poultry products because they are misbranded and may contain undeclared milk, egg, and soy.

    Product
    Amboy Group, LLC Recalls Poultry Products due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·18V872000·2018-12-07

    Mercedes-Benz Recalls 2018 C 300 and E 400 for Steering Defect

    Mercedes-Benz is recalling two 2018 vehicles because the steering coupling may not be locked, which could reduce steering ability and increase crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C 300, E 400
    Category
    Vehicle
    Distribution
    Distributed nationwide