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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4126–4150 of 6133

  • SevereFDA (Devices)·Z-0261-2023·2022-11-30

    3M Steri-Drape surgical drapes recalled due to adhesive skin injuries

    3M is recalling 103,000 units of Steri-Drape surgical drapes worldwide due to difficulties removing the adhesive liner and an increase in reported skin injuries from the adhesive.

    Product
    3M Steri-Drape, Medium Drape with Incise Film, REF 1060NS, general surgery drape
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0250-2023·2022-11-30

    3M Steri-Drape Surgical Drapes Recalled for Adhesive-Related Skin Injuries

    3M is recalling Steri-Drape surgical drapes (large towel drape, REF 1010) distributed worldwide. The affected drapes have reported adhesive-related skin injuries and a liner that is difficult to remove without damaging the product.

    Product
    3M Steri-Drape, Large Towel Drape, REF 1010, general surgery drape
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0259-2023·2022-11-30

    3M Steri-Drape Medium Drape Recalled for Adhesive Skin Injuries

    3M is recalling approximately 14,360 units of Steri-Drape surgical drapes due to adhesive-related skin injuries. The product's adhesive liner is difficult to remove and may render the drape unusable.

    Product
    3M Steri-Drape, Medium Drape with Wide Adhesive Aperture, REF 1033, general surgery drape
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0254-2023·2022-11-30

    3M Steri-Drape Surgical Drape Recall Due to Adhesive Injuries

    3M is recalling surgical drapes with defective adhesive components that may cause skin injuries. The adhesive liner is difficult to remove without damaging the product, and increased skin injuries have been reported.

    Product
    3M Steri-Drape, Small Drape with Adhesive Aperture, REF 1020NS, general surgery drape
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0257-2023·2022-11-30

    3M Steri-Drape surgical drapes recalled for adhesive liner defects and skin injuries

    3M is recalling Steri-Drape surgical drapes due to a defective adhesive liner that is difficult to remove and may render the drape unusable. Reported adhesive-related skin injuries have been linked to the affected lots.

    Product
    3M Steri-Drape, Medium Drape with Adhesive Aperture, REF 1030, general surgery drape
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0172-2023·2022-11-30

    Living Hydroponic Baby Romaine Lettuce Recalled Due to Salmonella Contamination Risk

    Kalera recalls Living Hydroponic Baby Romaine Lettuce (lot #001293) due to potential Salmonella contamination. The affected products comprise 211 cases of 10-pound packages distributed domestically.

    Product
    Living Hydroponic Baby Romaine Lettuce (10lbs)(04071) Kalera, Distributed by Kalera, Inc., Orlando, FL 32822 (Bulk)
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0170-2023·2022-11-30

    Kalera Butter Lettuce Recalled for Potential Salmonella Contamination

    Kalera butter lettuce (lot #001293 and #001294) is being recalled due to potential Salmonella contamination. Consumers should not consume the affected product.

    Product
    Kalera, The cleanest lettuce in the world., Butter lettuce, Whole head with living roots, Distributed by Kalera, Inc, Orlando FL 32822
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0237-2023·2022-11-30

    Mighty Bliss Electric Heating Pad Recalled for Burn and Shock Risk

    Whele LLC is recalling the Mighty Bliss Electric Heating Pad due to burn and shock hazards. The company has received complaints of burns, electrical shocks, and skin irritation.

    Product
    Mighty Bliss Electric Heating Pad, Extra-Large (20 x 24 ) Blue Electric Heating Pad, MB-002
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0264-2023·2022-11-30

    3M Urological Drape: Adhesive Liner Removal Issues and Skin Injuries

    3M has recalled 17,200 units of urological drapes due to adhesive liner removal difficulty and reported skin injuries. The affected drapes may become unusable in surgical settings.

    Product
    3M Steri-Drape, Urological Drape, REF 1071, general surgery (urology) drape
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0251-2023·2022-11-30

    3M Steri-Drape Surgical Drapes Recalled Due to Adhesive Defects and Skin Injuries

    3M is recalling Steri-Drape Large Towel Drapes (REF 1010NS) due to adhesive liner defects that may damage the product and increased reports of adhesive-related skin injuries from affected lots.

    Product
    3M Steri-Drape, Large Towel Drape, REF 1010NS, general surgery drape
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0249-2023·2022-11-30

    3M Steri-Drape surgical drapes recalled for skin injuries and adhesive damage

    3M is recalling 248,750 Steri-Drape surgical drapes used in medical facilities worldwide. The adhesive liner is difficult to remove without damaging the product, and there are reported increases in adhesive-related skin injuries.

    Product
    3M Steri-Drape, Small Towel Drape, REF 1000NSD, general surgery drape
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0256-2023·2022-11-30

    3M Steri-Drape Surgical Drape Recalled for Adhesive Skin Injuries

    3M Healthcare is recalling Steri-Drape surgical drapes due to an adhesive component that causes skin injuries and may render the product unusable. Affected: 104,000 units worldwide.

    Product
    3M Steri-Drape, Small Drape with Incise Film, REF 1021NS, general surgery drape
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0236-2023·2022-11-30

    Mighty Bliss Electric Heating Pad recalled for burn and shock hazards

    Whele LLC is recalling the Mighty Bliss Electric Heating Pad (model MB-001) due to burn and electrical shock hazards. The firm has received complaints of burns, shocks, and skin rashes from users.

    Product
    Mighty Bliss Electric Heating Pad, Large (12 x 24 ) Blue Electric Heating Pad, MB-001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0253-2023·2022-11-30

    3M Steri-Drape surgical drape recalled for adhesive liner defect and skin injuries

    3M is recalling 769,810 Steri-Drape surgical drapes worldwide due to a defective adhesive liner that is difficult to remove and has caused reported skin injuries.

    Product
    3M Steri-Drape, Small Drape with Adhesive Aperture, REF 1020, general surgery drape
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0248-2023·2022-11-30

    3M Steri-Drape surgical drapes recalled due to adhesive defect and skin injuries

    3M is recalling 504,000 units of Steri-Drape surgical drapes worldwide because the adhesive liner is difficult to remove and may damage the product. Reported cases of adhesive-related skin injuries have been associated with the affected lots.

    Product
    3M Steri-Drape, Small Towel Drape, REF 1000NS, general surgery drape
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0175-2023·2022-11-30

    Umami Everyday Savory Spice Recalled for Undeclared Soy

    Umami Everyday Savory Spice is recalled nationwide due to undeclared soy. The product affects consumers with soy allergies and has been distributed in the US, Canada, UK, and France.

    Product
    Umami Everyday Savory Spice, 5 fl. oz. (148 mL) glass bottle, UPC 8-50000-72724-3, Co-Packed with Seed Ranch Flavor Co., Denver, CO 80216 Ambient storage - minimum 35 degrees, maximum 85 degrees.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0262-2023·2022-11-30

    3M Steri-Drape General Surgery Drape Recall for Adhesive Skin Injuries

    3M is recalling 63,840 units of Steri-Drape surgical drapes worldwide due to reported adhesive-related skin injuries and defective protective liners that are difficult to remove without damaging the product.

    Product
    3M Steri-Drape, Medium Drape with Incise Film and Pouch, REF 1061, general surgery drape
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0255-2023·2022-11-30

    3M Steri-Drape surgical drape recalled due to adhesive skin injuries

    3M is recalling Steri-Drape surgical drapes because the liner on the adhesive component is difficult to remove without damaging the drape. An increase in adhesive-related skin injuries has been reported for affected lots.

    Product
    3M Steri-Drape, Small Drape with Incise Film, REF 1021, general surgery drape
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0173-2023·2022-11-30

    Smoked Salmon Recalled Due to Possible Listeria Contamination

    Wild caught Alaskan Sockeye smoked salmon may be contaminated with Listeria monocytogenes. Seven Seas International USA LLC is recalling 540 cases distributed to 164 retail stores.

    Product
    Wild caught Alaskan Sockeye Smoked Salmon NET WT 4 OZ (113g) EXPIRATION DATE 7-11-2024 UPC: 68826715832 Origin: USA, smoked and cured in The Netherlands
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0258-2023·2022-11-30

    3M Steri-Drape Surgery Drapes Recalled for Adhesive Liner and Skin Injuries

    3M is recalling 43,200 units of Steri-Drape surgical drapes due to a difficult-to-remove adhesive liner that may damage the product and reported increases in skin injuries.

    Product
    3M Steri-Drape, Medium Drape with Adhesive Aperture, REF 1030NS, general surgery drape
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0171-2023·2022-11-30

    Kalera Krunch Lettuce Recalled for Potential Salmonella Contamination

    Kalera is recalling Krunch lettuce (lots 001293 and 001294) due to potential Salmonella contamination. Consumers should dispose of affected products.

    Product
    Kalera, The cleanest lettuce in the world, Krunch lettuce, Whole head with living roots, Distributed by Kalera, Inc, Orlando FL 32822
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Drugs)·D-0066-2023·2022-11-23

    Hand Sanitizer Recalled for Methanol Contamination — FDA Class I

    Adam's Polishes ALCOHOL BASED HAND SANITIZER (multiple sizes) is recalled nationwide because FDA analysis found methanol contamination. This Class I recall poses a serious chemical health risk.

    Product
    Adam's Polishes ALCOHOL BASED HAND SANITIZER, isopropyl alcohol 75% v/v, packaged in a) 4 fl. oz (118) spray bottle, NDC 74943-125-04; b) 8 fl. oz (237 mL) spray bottle, NDC 74943-125-08; c) 1 PINT / 16 fl. oz (475 ml.) spray bottle, NDC 74943-125-16; and d) 1 GALLON / 128 fl. oz
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V870000·2022-11-23

    2023 IC Bus Models Suspension and Steering Fastener Recall

    Navistar is recalling 2023 IC Bus EV, CE, and RE models due to improperly heat-treated fasteners in suspension and steering joints. These fasteners may lose tension and cause steering instability, increasing crash risk.

    Product
    IC BUS — 2023 IC BUS EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V869000·2022-11-23

    International and IC Bus vehicles recalled for defective suspension and steering fasteners

    Navistar is recalling certain 2021-2023 International trucks and IC Bus vehicles because hex flange lock nuts in suspension and steering joints were improperly heat treated and may lose tension, creating a risk of steering instability.

    Product
    INTERNATIONAL — 2023 INTERNATIONAL HV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0151-2023·2022-11-23

    Zingerman's Pumpkin Gelato Recalled for Undeclared Egg Allergen

    Zingerman's Creamery is recalling Harvest Pumpkin Gelato due to undeclared egg allergen. The recall affects pints and quarts distributed in Michigan.

    Product
    Zingerman's Harvest Pumpkin Gelato pint (16oz) and quart (32oz) sizes
    Category
    Food
    Distribution
    1 state