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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19226–19250 of 39605

  • SevereFDA (Devices)·Z-0143-2018·2017-11-29

    Exactech Recalls Optetrak Offset Tibial Tray Due to Design Incompatibility

    Exactech is recalling 333 Optetrak Offset Tibial Tray and Screws units due to a design incompatibility with certain offset spine stiffener screws and constrained condylar tibial inserts.

    Product
    Optetrak Offset Tibial Tray and Screws, Size 5F/4T, Beta, Ref 208-04-52, Sterile, RX.
    Category
    Medical Device
    Distribution
    11 states
  • SevereFDA (Devices)·Z-0126-2018·2017-11-29

    Exactech Recalls Optetrak Offset Tibial Trays Due to Design Incompatibility

    Exactech is recalling 57 Optetrak Offset Tibial Trays and Screws due to a design incompatibility with certain offset spine stiffener screws and constrained condylar tibial inserts.

    Product
    Optetrak Offset Tibial Tray and Screws, Size 0F/0T, Alpha, Ref 208-04-01, Sterile, RX.
    Category
    Medical Device
    Distribution
    11 states
  • SevereFDA (Devices)·Z-0072-2018·2017-11-29

    Spacelabs Arkon Anesthesia Workstation Recalled for Mechanical and Display Failures

    Spacelabs Healthcare is recalling 110 Arkon Anesthesia Workstations due to failures in ventilation, gas delivery, and display alarms.

    Product
    Arkon Anesthesia Delivery System, Model 99999, and software version 2.61 and upgrade kit 050-9043-00 Rev G. The Spacelabs Arkon Anesthesia Workstation is intended for use in the hospital environment and operating room. It may be used for the delivery of oxygen, air and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0144-2018·2017-11-29

    Exactech Recalls Optetrak Offset Tibial Tray Due to Design Incompatibility

    Exactech is recalling 317 Optetrak Offset Tibial Trays because a design incompatibility exists with certain offset spine stiffener screws and constrained condylar tibial inserts.

    Product
    Optetrak Offset Tibial Tray and Screws, Size 5F/5T, Alpha, Ref 208-04-53, Sterile, RX.
    Category
    Medical Device
    Distribution
    11 states
  • SevereFDA (Food)·F-0393-2018·2017-11-29

    Dilettante Chocolates Espresso Blend Recalled for Undeclared Almonds

    Seattle Gourmet Foods Inc. is recalling Dilettante Chocolates Espresso Blend sold at Costco because it may contain undeclared almonds.

    Product
    Dilettante Chocolates Espresso Blend, Espresso Beans in Semisweet, Milk and White Chocolate., Costco item # 2335. The product is packaged in a clear plastic bag, net weight 5-pounds and has the UPC 37041 05211. The product label is read in parts: "***Dilettante Chocolates…
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·17V768000·2017-11-29

    Ford Recalls 2017 F-53 and F-59 Chassis for Brake Fluid Leak Risk

    Ford is recalling 2017 F-53 and F-59 chassis because missing plugs in the brake control unit may cause fluid leaks or air ingestion, increasing stopping distance.

    Product
    FORD — FORD F-59, F-53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V766000·2017-11-29

    Volkswagen Recalls 2018 Atlas Vehicles Due to Fuel Tank Leak Risk

    Volkswagen is recalling 2018 Atlas vehicles because the fuel tank may have insufficient wall thickness, potentially causing a fuel leak and increasing fire risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0385-2018·2017-11-29

    Woodstock Farms Dark Chocolate Cashews Recalled for Missing Milk Labeling

    United Natural Trading Inc. is recalling Market Basket Dark Chocolate Cashews because the label failed to list milk fat as an ingredient or include a 'contains milk' statement.

    Product
    Market Basket Dark Chocolate Cashews 8/12oz.
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0365-2018·2017-11-22

    West Creek BBQ Sauce Recalled for Undeclared Egg

    CFS West Holdings Inc. is recalling West Creek Original BBQ Sauce because it may contain undeclared egg.

    Product
    West Creek Original BBQ Sauce, Net Contents 1 Gal, Distributed by Performance Food Group, Richmond, VA packaged in plastic jugs.
    Category
    Food
    Distribution
    12 states
  • CriticalFDA (Food)·F-0253-2018·2017-11-22

    Meijer Recalls Mixed Pepper Blend Due to Listeria Contamination Risk

    Meijer Distribution is voluntarily recalling mixed pepper blend and other vegetable products due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Vegetable products including: MIXED PEPPER BLEND
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-0247-2018·2017-11-22

    Meijer Recalls Cauliflower Florets Due to Listeria Contamination Risk

    Meijer Distribution is voluntarily recalling specific cauliflower floret products due to potential Listeria monocytogenes contamination identified by a supplier.

    Product
    Vegetable products including: CAULIFLOWER FLORETS 3 LB BAG CAULIFLOWER FLORETTS (EDI) CAULIFLOWER FLORETTS CAULIFLOWER FLORETS PLU 4566 PRE-PACKAGED CAULIFLOWER FLORETS CAULI FLORETS 3 LB BAG CAULIFLOWER FLORETTS LB
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-0367-2018·2017-11-22

    Texas Roadhouse Barbecue Sauce Recalled for Undeclared Egg

    CFS West Holdings Inc is recalling Texas Roadhouse Barbecue Sauce because it may contain undeclared egg. The product was distributed to distributors in 12 states.

    Product
    Texas Roadhouse Barbecue Sauce, NET 3/2 gallon, Mfg. exclusively for: Texas Roadhouse Restaurants, Louisville, KY, packaged in plastic pouches.
    Category
    Food
    Distribution
    12 states
  • CriticalFDA (Food)·F-0248-2018·2017-11-22

    Meijer Recalls Salad Rotini Mozzarella Medley Due to Listeria Risk

    Meijer is voluntarily recalling specific salad rotini products due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Vegetable products including: Markets of Meijer SALAD ROTINI MOZZARELLA MEDLEY, Markets of Meijer SALAD ROTINI MOZZARELLA MEDLEY G&G
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0243-2018·2017-11-22

    Etai's Recalls Caprese Panini and Veggie Wrap for Undeclared Tree Nuts

    Etai's Food, Inc. is recalling Caprese Panini and Veggie Wrap products due to undeclared tree nuts, a potential allergen hazard.

    Product
    Caprese Panini, Net WT: 7 oz/198g, UPC 7 62089 10728 4, Etai's, individual plastic container, keep under refrigeration
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0252-2018·2017-11-22

    Meijer Recalls Zucchini Squash Due to Listeria Contamination Risk

    Meijer Distribution is voluntarily recalling zucchini squash and other vegetable products due to potential Listeria monocytogenes contamination.

    Product
    Vegetable products including: ZUCCHINI SQUASH
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0076-2018·2017-11-22

    Amneal Recalls Fosphenytoin Sodium Injection Due to Particulate Matter

    Amneal Pharmaceuticals is recalling 14,000 vials of Fosphenytoin Sodium Injection because of the presence of particulate matter.

    Product
    Fosphenytoin Sodium Injection, USP, 500 mg PE/10 mL (50 mg PE/mL. 10 mL Single Dose Vial, Rx Only. Distributed by: Amneal Biosciences, Bridgewater, NJ 08807. NDC: 70121-1390-7
    Category
    Drug
    Distribution
    5 states
  • SevereFDA (Drugs)·D-0080-2018·2017-11-22

    PharMEDium Recalls Hydromorphone Injection Due to Potency Failure

    PharMEDium Services is recalling 499 syringes of Hydromorphone HCl injection because the product failed potency specifications.

    Product
    Hydromorphone HCl 0.5 mg per mL in 0.9% Sodium Chloride Injection 1 mL, packaged in syringes, Rx Only , PharMEDium Services, LLC. 913 N. Davis Ave Cleveland, MS 38732, NDC 61553-352-40
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Food)·F-0244-2018·2017-11-22

    Etai's Recalls Veggie Wrap and Caprese Panini for Undeclared Tree Nuts

    Etai's Food, Inc. is recalling specific lots of Veggie Wrap and Caprese Panini due to undeclared tree nuts, posing a risk to consumers with allergies.

    Product
    Veggie Wrap, Net Wt: 8 oz/227g, UPC 7 62089 10655 3, Etai's, individual plastic container, keep under refrigeration
    Category
    Food
    Distribution
    0 states