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 deaths or serious injuries are reported, 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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10601–10625 of 36632

  • CriticalFDA (Food)·F-1607-2020·2020-10-07

    Spokane Produce Recalls Sliced Onions Due to Salmonella Newport Risk

    Spokane Produce, Inc. is recalling refrigerated sliced onions due to a potential Salmonella Newport contamination. The product was distributed in five western states.

    Product
    Item 79090 Onion Yellow Sliced, Refrigerated, net wt. 5 LB, packaged in Sealed Plastic Bag. No label. Item 79100 Onion Yellow Sliced, Refrigerated, net wt. 5 LB, packaged in Sealed Plastic Bag. No label.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1608-2020·2020-10-07

    Spokane Produce Recalls Slivered Onions Due to Salmonella Newport Risk

    Spokane Produce, Inc. is recalling 5-pound bags of sliced yellow onions because they may contain Salmonella Newport. The product was distributed in five western states.

    Product
    Item 79391 Onion Yellow Slivered, Refrigerated, net wt. 5 LB, packaged in Sealed Plastic Bag. No label.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1565-2020·2020-10-07

    Spokane Produce Recalls Spicy Thai Peanut Salad Kit Due to Salmonella

    Spokane Produce, Inc. is recalling refrigerated Spicy Thai Peanut Salad Kits because the onion ingredient may be contaminated with Salmonella Newport.

    Product
    Item 80208 Spicy Thai Peanut Salad Kit, Refrigerated, net wt. 3.9 LB, packaged in Cardboard Box.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Drugs)·D-0029-2021·2020-10-07

    Blumen Hand Sanitizer Recalled for Methanol and Low Alcohol Content

    4e Brands North America is recalling Blumen hand sanitizer bottles and pumps found to contain methanol and less ethanol than labeled.

    Product
    blumen Clear ADVANCED HAND SANITIZER with 70% ALCOHOL, (ethyl alcohol 70% v/v), Packaged as a) 2 fl oz / 60 ml bottle, UPC 8 14266 02371 6 b) 17 fl oz / 503 ml bottle with blue cap or pump bottle, UPC 8 14266 02409 6 c) 33.8 fl oz / 1 L straight or curved bottle, UPC 8 14266 0236
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1592-2020·2020-10-07

    Spokane Produce Recalls Unlabeled Refrigerated Dinner Mix Due to Salmonella Risk

    Spokane Produce, Inc. is recalling 35 pounds of unlabeled, refrigerated dinner mix due to a potential Salmonella Newport contamination from onion ingredients.

    Product
    Item 80743 DINNER MIX, Refrigerated, net wt. 5 LB, packaged in Sealed Plastic Bag. No label.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1558-2020·2020-10-07

    Spokane Produce Recalls Macaroni Salad Kit Due to Salmonella Risk

    Spokane Produce, Inc. is recalling refrigerated macaroni salad kits because they contain onion supplied by a source linked to Salmonella Newport.

    Product
    Item 80732 MFB Macaroni Salad Kit, Refrigerated, net wt. 7.78 LB, packaged in Cardboard Box.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1572-2020·2020-10-07

    Spicy Thai Peanut Wrap Recalled for Salmonella Newport Contamination

    Spokane Produce, Inc. is recalling Spicy Thai Peanut Wraps due to Salmonella Newport contamination from onion supplied by Thomson International, Inc.

    Product
    Item 80212 Spicy Thai Peanut Wrap, Refrigerated, net wt. 11 OZ, packaged in Plastic Wrapped.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1605-2020·2020-10-07

    Spokane Produce Recalls Unlabeled Yellow Onion Kabobs for Salmonella Risk

    Spokane Produce, Inc. is recalling 45 pounds of unlabeled, refrigerated yellow onion kabobs due to a potential Salmonella Newport contamination. The product was distributed in Idaho, Montana, Oregon, Washington, and Wyoming.

    Product
    Item 79020 Onion Yellow Kabob, Refrigerated, net wt. 5 LB, packaged in Plastic Wrapped. No label.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1588-2020·2020-10-07

    Spokane Produce Recalls Pico De Gallo Salsa Due to Salmonella Newport

    Spokane Produce, Inc. is recalling two Pico De Gallo Salsa products because they contain onion supplied from Thomson International, Inc. that may be contaminated with Salmonella Newport.

    Product
    Item 83981 Pico De Gallo Salsa Med Saddlin' Up, Refrigerated, net wt. 16 OZ, packaged in Plastic Container. Item 83988 Pico De Gallo Salsa Med, net wt. 32 OZ, packaged in Plastic Container.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1580-2020·2020-10-07

    Spokane Produce Guacamole Pico Recalled for Salmonella Newport Risk

    Spokane Produce, Inc. is recalling 12-ounce refrigerated Guacamole Pico containers due to potential Salmonella Newport contamination from onion ingredients.

    Product
    Item 80816 Guacamole Pico, Refrigerated, net wt. 12 OZ, packaged in Plastic Container.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1567-2020·2020-10-07

    Spokane Produce Recalls Cucumber Red Onion Salad Kits for Salmonella

    Spokane Produce, Inc. is recalling refrigerated Cucumber Red Onion Salad Kits due to potential Salmonella Newport contamination from onion ingredients.

    Product
    Item 80624 Cucumber Red Onion Salad Kit, Refrigerated, net wt. 6.6 LB, packaged in Cardboard Box.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1554-2020·2020-10-07

    Spokane Produce Recalls Citrus Kale Salad Kits for Salmonella Newport

    Spokane Produce, Inc. is recalling refrigerated Citrus Kale Salad Kits due to potential Salmonella Newport contamination from onion supplied by Thomson International, Inc.

    Product
    Item 80747 Citrus Kale Salad Kit, Refrigerated, net wt. 5.62 LB, packaged in Cardboard Box.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1557-2020·2020-10-07

    Spokane Produce Recalls Delux Macaroni Salad Due to Salmonella Newport Risk

    Spokane Produce, Inc. is recalling refrigerated Delux Macaroni Salad because it contains onion supplied by Thomson International, Inc., which is associated with Salmonella Newport.

    Product
    Item 80739 Delux Macaroni Salad, Refrigerated, net wt. 7 LB, packaged in Cardboard Box.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1591-2020·2020-10-07

    Spokane Produce Recalls Asparagus and Mixed Vegetables Due to Salmonella Risk

    Spokane Produce, Inc. is recalling refrigerated asparagus and mixed vegetables due to potential Salmonella Newport contamination from onion ingredients.

    Product
    Item 80819 ASPARAGUS w/ Mixed Vegetables, Refrigerated, net wt. 10 OZ, packaged in Sealed Plastic Bag. No label.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1615-2020·2020-10-07

    Spokane Produce Super Stir Fry Package Recalled for Salmonella Newport

    Spokane Produce, Inc. is recalling refrigerated Super Stir Fry Packages due to the presence of Salmonella Newport in the onion ingredient.

    Product
    Item 80845 Super Stir Fry Package, Refrigerated, net wt. 16 OZ, packaged in Sealed Plastic Bag. Label does not have cooking instructions.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1547-2020·2020-10-07

    Spokane Produce Recalls Greek Salad Due to Salmonella Newport Risk

    Spokane Produce, Inc. is recalling refrigerated Greek Salad items because they contain onion supplied from Thomson International, Inc. that may be contaminated with Salmonella Newport.

    Product
    Item 80573 Greek Salad w/ Italian Dressing, Refrigerated, net wt. 6.5 OZ, packaged in Plastic Container. Item 80572 Greek Salad, Refrigerated, net wt. 11 OZ, packaged in Plastic Container.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1600-2020·2020-10-07

    Spokane Produce Recalls Unlabeled Diced Onions Due to Salmonella Newport

    Spokane Produce, Inc. is recalling unlabeled diced onions distributed in the Pacific Northwest and Mountain West due to a Salmonella Newport hazard.

    Product
    Item 78800 Onion White Diced, Refrigerated, net wt. 5 LB, packaged in Sealed Plastic Bag. No label. Item 78801 Onion White Diced, Refrigerated, net wt. 2 LB, packaged in Sealed Plastic Bag. No label.
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-0008-2021·2020-10-07

    Endo GIA Stapler Recall Due to Incomplete Staple Formation

    FDA recalls Endo GIA Auto Suture staplers because staples may not form properly, potentially preventing adequate hemostasis during surgery.

    Product
    Endo GIA Auto Suture Universal Articulating Loading Unit 60 mm - 3.5 mm, Item Code 030458 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0031-2021·2020-10-07

    Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures

    Riverpoint Medical is recalling 1,264 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.

    Product
    Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 5/0 Undyed 30" KV-11, TaperCutting, Product Number: CV2293, UDI: 20884521151588 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0032-2021·2020-10-07

    Losartan Pot/HCTZ 50/12.5 mg Recalled Due to Impurity Detection

    Direct Rx is recalling 33 bottles of Losartan Pot/HCTZ 50/12.5 mg tablets distributed in Florida due to trace amounts of impurity NMBA.

    Product
    Losartan Pot/HCTZ 50/12.5 mg 90 Tabs Packaged and Distributed By: Direct Rx Dawsonville, GA 30534 Mfg For: Torrent Pharma, Inc. Basking Ridge, NJ 07920 NDC 61919-040-90
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Devices)·Z-3053-2020·2020-10-07

    ESAOTE Portable Ultrasound AC/DC Power Supply Recall for Overheating Risk

    ESAOTE is recalling AC/DC power supplies for specific portable ultrasound systems because the connector may heat up, generate smoke, and melt.

    Product
    AC/DC POWER SUPPLY for 7400, Part Number 151004301, XP Power Model Number AHM180PS19-XE1057, AC/DC Adapter associated with the following portable ultrasound diagnostic systems: The AC/DC adapter is intended for use with the following portable ultrasound systems: MyLabAlpha (1017
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0022-2021·2020-10-07

    Blumen Hand Sanitizer Recalled for CGMP Deviations and Methanol Risk

    4e Brands North America is recalling Blumen Advanced Instant Hand Sanitizer due to manufacturing in a facility associated with methanol contamination.

    Product
    blumen ADVANCED INSTANT HAND SANITIZER Clear ETHYL ALCOHOL 70% Natural Boost with Tea Tree Oil, (70% ethyl alcohol), Packaged as a) 18 fl oz / 532 ml bottle, UPC 8 14266 02408 9 b) 33.8 fl oz / 1L bottle, UPC 8 14266 02374 7, Distributed in USA and Canada BY: 4e Brands Northamer
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0023-2021·2020-10-07

    Blumen Hand Sanitizer Recalled for CGMP Deviations and Methanol Risk

    4e Brands North America is recalling Blumen Advanced Hand Sanitizer due to manufacturing in a facility associated with methanol contamination.

    Product
    blumen ADVANCED HAND SANITIZER, 70% ALCOHOL CONTENT, (70% ethyl alcohol), packaged as a) 3.4 fl oz / 100 ml bottle, UPC 8 14266 02359 4 b) 7.5 fl. oz./221 ml bottle, UPC 8 14266 02362 4 b) 33.8 fl. oz./1L bottle, UPC 8 14266 02369 3, Distributed in USA and Canada By: 4e Brands No
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·21004·2020-10-07

    CB2 Recalls Bordo Dining Tables Due to Collapse Hazard

    CB2 is recalling Bordo and Bordo XL dining tables because the legs can become unsteady, causing the table to collapse and posing an injury hazard.

    Product
    Bordo and Bordo XL dining tables
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0048-2021·2020-10-07

    Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures

    Riverpoint Medical is recalling non-sterile Velosorb Fast Braided Absorbable Sutures due to a risk of surgical site infection.

    Product
    Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30" P-14 Cutting SV935, UDI: 20884521151755 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligat
    Category
    Medical Device
    Distribution
    Distributed nationwide