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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12126–12150 of 36637

  • SevereFDA (Devices)·Z-0780-2020·2020-01-15

    Stryker T2 Alpha Delta Strike Plate Recalled for Breakage Risk

    Stryker GmbH is recalling T2 Alpha Delta Strike Plate instruments because they can break during nail implantation or removal, potentially causing complications.

    Product
    Stryker T2 Alpha Delta Strike Plate IMN Instruments - part of the IMN Instruments System and is used to support insertion and withdrawal of nails through the Targeting Device Catalog Number: 2351-0050
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0495-2020·2020-01-15

    Reichel Foods Recalls Pro2Snax Snack Trays Due to Listeria Contamination

    Reichel Foods Inc. is recalling Pro2Snax To The Max snack trays due to Listeria monocytogenes contamination. The affected products were distributed nationwide.

    Product
    Pro2Snax To The Max snack tray containing Sliced Apples, Hard Boiled Egg, Mild Cheddar Cheese, and Dried Cranberries & Cashews. Item # 1-4555-6. Net Wt. 7.35 oz (208g) UPC 6 49632-00149 0 Keep Refrigerated.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V010000·2020-01-10

    Genuine Scooter Recalls 2020 Royal Alloy GT150 Due to Brake Rotor Defect

    Genuine Scooters is recalling 2020 Royal Alloy GT150 scooters because the front brake rotor may become uncentered, potentially causing a loss of braking and increasing crash risk.

    Product
    GENUINE SCOOTER — GENUINE SCOOTER ROYAL ALLOY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·002-2020·2020-01-10

    Culinary International Recalls Chicken Burritos Due to Undeclared Egg Allergen

    Culinary International is recalling approximately 626 pounds of frozen chicken burritos that actually contain eggs, an undeclared allergen. No illnesses have been reported.

    Product
    Ruiz Food Products, Inc. — Culinary International, LLC Recalls Chicken Burrito Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V011000·2020-01-10

    GM Recalls 2007-2008 Trucks for Air Bag Inflator Defect

    General Motors is recalling 2007-2008 Chevrolet Silverado and GMC Sierra trucks because front passenger air bag inflators may explode.

    Product
    GMC — GMC, CHEVROLET SIERRA 2500, SIERRA 3500, SILVERADO 2500, SILVERADO 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·20V007000·2020-01-09

    Ferrari Recalls 458 Italia and California for Air Bag Defect

    Ferrari is recalling 982 vehicles because front passenger air bag inflators may explode, posing a risk of serious injury or death.

    Product
    FERRARI — FERRARI CALIFORNIA, 458 ITALIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·20V008000·2020-01-09

    Nissan and Infiniti Recall Vehicles for Air Bag Inflator Defect

    Nissan is recalling specific 2001-2011 Nissan and Infiniti vehicles because front passenger air bag inflators may explode due to propellant degradation.

    Product
    INFINITI — INFINITI, NISSAN M45, QX4, I30, I35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0633-2020·2020-01-08

    FDA Recalls Silver Bullet Male Enhancement Capsules for Undeclared Active Ingredient

    The FDA is recalling Silver Bullet male enhancement capsules because they contain an undeclared active ingredient (Sildenafil) and were marketed without an approved NDA/ANDA.

    Product
    Silver Bullet, Get Bigger and Harder, Works in Minutes, Lasts for Days, 10 male enhancement capsules in blister foil package, 725mg per capsule, Distributed by Silver Bullet Ltd, Golden Springs, CO, USA, UPC: 610877392698.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0746-2020·2020-01-08

    Thoratec HeartMate 3 Mobile Power Unit Recalled for Static Electricity Risk

    Thoratec Corp. is recalling HeartMate 3 Mobile Power Units because excessive static electricity can cause unrecoverable power loss, potentially reducing blood flow from the left ventricular assist system.

    Product
    HeartMate 3 Mobile Power Unit, REF 107754, UDI or GTIN: 00813024010883, and 107758, UDI or GTIN: 00813024010890, when connected to the HeartMate 3 Left Ventricular Assist System, REF 106524US, UDI or GTIN: 00813024013297, and 106524, UDI or GTIN: 00813024011712 - Product Usage…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0632-2020·2020-01-08

    Ranitidine Tablets Recalled Due to NDMA Impurity

    Granules India Limited is recalling Ranitidine tablets because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).

    Product
    RANITIDINE — RANITIDINE (RANITIDINE)
    Category
    Drug
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0631-2020·2020-01-08

    American Health Packaging Recalls Ranitidine Syrup Due to NDMA Impurity

    American Health Packaging is recalling specific lots of Ranitidine Syrup because the presence of the NDMA impurity was detected in the product.

    Product
    Ranitidine Syrup (Ranitidine Oral Solution USP), 15 mg/mL, 150 mg/10 mL per cup, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio. (a) Case of 50 cups (NDC 60687-260-69) (b) Case of 40 cups (NDC 60687-260-23 (c) Unit Dose Cup (NDC 60687-260-69)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·001-2020·2020-01-03

    Kettle Cuisine Recalls Lentil and Beef Soup for Undeclared Allergens

    Kettle Cuisine Midco, LLC is recalling ready-to-eat lentil and beef soup products because they contain undeclared egg and wheat allergens.

    Product
    Kettle Cuisine Midco, LLC — Kettle Cuisine Midco, LLC, Recalls Ready-To-Eat Soup Products due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    6 states
  • CriticalNHTSA·20V001000·2020-01-02

    Subaru and Saab Vehicles Recalled for Air Bag Inflator Defect

    Subaru is recalling specific 2003-2014 models and Saab 9-2X vehicles because passenger air bag inflators may explode due to humidity, posing a risk of serious injury or death.

    Product
    SUBARU — SUBARU, SAAB OUTBACK, BAJA, IMPREZA, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E001000·2020-01-02

    Takata Frontal Air Bag Inflators Recalled for Explosion Risk

    Takata is recalling specific non-desiccated frontal air bag inflators used as interim remedies. These inflators may explode due to propellant degradation, posing a risk of serious injury or death.

    Product
    AIR BAGS:FRONTAL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V003000·2020-01-02

    Subaru and Saab Recall Vehicles Due to Air Bag Inflator Defect

    Subaru is recalling specific 2003-2014 models and Saab 9-2X vehicles because passenger air bag inflators may explode, posing a risk of serious injury or death.

    Product
    SUBARU — SUBARU, SAAB OUTBACK, BAJA, IMPREZA, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V002000·2020-01-02

    Subaru and Saab Recall Vehicles Due to Air Bag Inflator Defect

    Subaru and Saab are recalling specific model years because passenger air bag inflators may explode due to humidity, posing a risk of serious injury.

    Product
    SUBARU — SUBARU, SAAB OUTBACK, BAJA, IMPREZA, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0417-2020·2020-01-01

    FDA Recalls Okami California Rolls for Listeria Contamination Risk

    Fuji Food Products is recalling Okami brand 8pc California Rolls due to potential Listeria monocytogenes contamination. Consumers should not eat the product.

    Product
    Okami brand 8pc California Roll, SKU 28101
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Food)·F-0422-2020·2020-01-01

    FDA Recalls Okami Spicy Supreme California Rolls for Listeria Risk

    Fuji Food Products is recalling Okami brand 8pc Spicy Supreme California Rolls due to potential Listeria monocytogenes contamination.

    Product
    Okami brand 8pc Spicy Supreme California Roll, SKU 28104
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Food)·F-0414-2020·2020-01-01

    Trader Joe's Tempura Shrimp Crunch Roll Recalled for Listeria Risk

    Fuji Food Products is recalling Trader Joe's 8pc Tempura Shrimp Crunch Roll due to potential Listeria monocytogenes contamination.

    Product
    Trader Joe's 8pc Tempura Shrimp Crunch Roll, 8.5oz, SKU 513289
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Devices)·Z-0022-2020·2020-01-01

    Galemed Babi.Plus Pressure Relief Manifold Recalled for Low Venting Pressure

    Galemed is recalling Babi.Plus 12.5 cm H2O Pressure Relief Manifolds because they may vent gas below standard pressure. The recall covers 14,964 units distributed in North Carolina and Nevada.

    Product
    Babi.Plus 12.5 cm H2O Pressure Relief Manifold with Gas Supply Tube and Oxygen Sensor Port, REF 2691, Rx Only, UDI: 04710810100802
    Category
    Medical Device
    Distribution
    2 states
  • CriticalFDA (Food)·F-0413-2020·2020-01-01

    Trader Joe's California Rolls Recalled for Listeria Risk

    Fuji Food Products is recalling Trader Joe's 8pcs Regular California Rolls due to potential Listeria monocytogenes contamination.

    Product
    Trader Joe's 8pcs Regular California Roll, 8oz, SKU 00348997T
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Food)·F-0416-2020·2020-01-01

    Trader Joe's Brown Rice California Rolls Recalled for Listeria Risk

    Fuji Food Products is recalling Trader Joe's Brown Rice California Rolls due to potential Listeria monocytogenes contamination.

    Product
    Trader Joe's 8pcs Brown Rice California Roll, 8oz, SKU 909822
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Food)·F-0430-2020·2020-01-01

    Trader Joe's Smoked Salmon Poke Bowl Recalled for Listeria Risk

    Fuji Food Products is recalling Trader Joe's 8.4oz Smoked Salmon Poke Bowls due to potential Listeria monocytogenes contamination.

    Product
    Trader Joe's 8.4oz Smoked Salmon Poke Bowl, SKU 603751
    Category
    Food
    Distribution
    31 states