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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9101–9125 of 27441

  • 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-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-0238-2023·2022-11-30

    Mighty Bliss Electric Heating Pad recalled due to burn and shock hazard

    Whele LLC is recalling approximately 4,034 Mighty Bliss Electric Heating Pads due to burn and shock hazards. The firm received complaints of burns, mild electrical shocks, and skin irritation.

    Product
    Mighty Bliss Electric Heating Pad, Large (12 x 24 ) Grey Electric Heating Pad, PE-MtyBls-HeatPad-12x24-Gry-V2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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-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-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 (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 (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-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-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-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-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-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 (Devices)·Z-0263-2023·2022-11-30

    3M Steri-Drape Surgical Drape Recall for Adhesive Defect and Skin Injuries

    3M is recalling 554,200 surgical drapes due to a difficult-to-remove adhesive liner that may damage the product and render it unusable. The company has received reports of adhesive-related skin injuries from the affected lots.

    Product
    3M Steri-Drape, Medium Drape with Incise Film and Pouch, REF 1061NS, general surgery 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-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
  • HighFDA (Devices)·Z-0302-2023·2022-11-30

    Surgical Convenience Kits with Recalled 3M Surgical Drapes

    ROi CPS LLC is recalling 21 surgical convenience kits distributed to Louisiana, Missouri, North Carolina, and Florida because they contain 3M surgical drapes that were subsequently recalled.

    Product
    regard SPINE , NU00974F, Item Number 800769006; neuro surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0293-2023·2022-11-30

    Surgical convenience kits recalled due to defective surgical drapes

    Regard MAJOR EAR surgical convenience kits distributed in Louisiana, Missouri, North Carolina, and Florida are being recalled because the kits contained 3M surgical drapes that were subsequently recalled.

    Product
    regard MAJOR EAR, ET00326J, Item Number 800070010; ear surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0318-2023·2022-11-30

    Regard Shoulder surgical kits recalled due to defective included drapes

    ROi CPS LLC is recalling Regard SHOULDER surgical convenience kits because they contain 3M surgical drapes that were subsequently recalled. Affected kits were distributed to healthcare facilities in LA, MO, NC, and FL.

    Product
    regard SHOULDER, GS00828G, Item Number 880367007; ortho surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0282-2023·2022-11-30

    VS3 Iridium Visionsense Beam Combiner Optical Fiber Cable Damage Risk

    Visionsense VS3 Iridium beam combiners may develop damaged optical fiber cables through handling or bending, causing loss of functionality and potential cable heating or melting. Affected units were distributed nationwide in the US.

    Product
    VS3 Iridium Visionsense Infrared (IR) Fluorescence Light Integrator (Beam Combiner) Product Number: 161-0001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0260-2023·2022-11-30

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

    3M recalls specific batches of Steri-Drape surgical drapes due to reported adhesive-related skin injuries and potential product damage from difficult-to-remove adhesive liners.

    Product
    3M Steri-Drape, Medium Drape with Incise Film, REF 1060, general surgery drape
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0309-2023·2022-11-30

    Surgical Convenience Kits Recalled Due to Included 3M Surgical Drapes

    Surgical convenience kits are being recalled because they contained 3M surgical drapes that were subsequently recalled. 177 kits distributed in Louisiana, Missouri, North Carolina, and Florida are affected.

    Product
    regard SHOULDER PACK, GS00125V, Item Number 880120022; ortho surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0247-2023·2022-11-30

    3M Steri-Drape surgical drape with defective adhesive liner recalled

    3M is recalling Steri-Drape Small Towel Drapes because the adhesive liner is difficult to remove without damaging the product and has caused reported skin injuries.

    Product
    3M Steri-Drape, Small Towel Drape, REF 1000, general surgery drape
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0283-2023·2022-11-30

    Regard LAMINECTOMY surgical kits recalled due to recalled 3M drapes

    ROi CPS LLC is recalling Regard LAMINECTOMY surgical convenience kits because they contain 3M surgical drapes that were subsequently recalled.

    Product
    regard LAMINECTOMY, NU01140, Item Number 900940; neuro surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0285-2023·2022-11-30

    Surgical Convenience Kits Recalled Due to Included Recalled Surgical Drapes

    ROi CPS LLC is recalling 326 regard TOTAL JOINT surgical convenience kits distributed in Louisiana, Missouri, North Carolina, and Florida. The kits contain 3M surgical drapes that were previously recalled. No illnesses or injuries have been reported.

    Product
    regard TOTAL JOINT, OR00446F, Item Number 880291; orthopedic surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states