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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10776–10800 of 13816

  • 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-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-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-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-0280-2023·2022-11-30

    Visionsense Infrared Microscope Recalled Due to Optical Fiber Cable Damage

    Visionsense is recalling 205 units of its VS3 Iridium microscope because optical fiber cables may become damaged during handling, causing loss of function and outer cable heating or melting.

    Product
    VS3 Iridium Visionsense Infrared (IR) Fluorescence Miniature Microscope (MMS-IR) Product Number: 174-0012
    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-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-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-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-0311-2023·2022-11-30

    Neuro surgery kits recalled for defective 3M surgical drapes

    ROi CPS LLC is recalling 790 neuro surgery convenience kits that contained 3M surgical drapes which were subsequently recalled. The kits were distributed to Louisiana, Missouri, North Carolina, and Florida.

    Product
    regard MINOR NEURO, NU00140AD, Item Number 880135030; neuro surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0272-2023·2022-11-30

    Medfusion 4000 Syringe Pump May Delay Sending EHR Infusion Start Messages

    Smiths Medical's Medfusion 4000 infusion pump software may delay sending infusion start messages to Electronic Health Record systems, potentially affecting infusion programming and clinical documentation.

    Product
    Medfusion Model 4000 Syringe Infusion Pump, with software versions V1.6.0 or V1.6.1 that have implemented the Smart Pump Programming (SPP) feature in a clinical treatment environment. Used for infusion of fluids requiring precisely controlled infusion rates including blood or
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0267-2023·2022-11-30

    Ventilator Screen Backlight Malfunction Causes Temporary Display Loss

    Hamilton-C6 ventilators are subject to a backlight malfunction causing the display screen to go black for 2-3 seconds. The FDA has classified this Class II recall as affecting 443 U.S. systems distributed nationwide.

    Product
    Hamilton-C6
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0252-2023·2022-11-30

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

    3M is recalling 84,000 units of Steri-Drape surgical drapes because the adhesive component's liner is difficult to remove without damaging the product, and there have been reported adhesive-related skin injuries.

    Product
    3M Steri-Drape, Large Towel Drape, REF 1010NSD, general surgery drape
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0317-2023·2022-11-30

    Surgical Urology Kits Recalled Due to Defective 3M Drapes

    ROi CPS LLC is recalling 166 Regard Pediatric Urology surgical convenience kits distributed in Louisiana, Missouri, North Carolina, and Florida. The kits contained 3M surgical drapes that were subject to a separate recall.

    Product
    regard PEDIATRIC UROLOGY, GS00467J, Item Number 880306010; uro surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0316-2023·2022-11-30

    Eye Surgery Convenience Kits Recalled for Defective Surgical Drapes

    Cataract eye surgery convenience kits containing recalled 3M surgical drapes were distributed to four states. ROi CPS LLC has recalled 780 units of the regard CATARACT product.

    Product
    regard CATARACT, EY00450L, Item Number 880295012; eye surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0296-2023·2022-11-30

    Surgical Convenience Kits Recalled Due to Included 3M Drape Components

    Orthopaedic surgical convenience kits distributed in four states contained 3M surgical drapes that were subsequently recalled. ROi CPS LLC is recalling 38 affected kits.

    Product
    regard HAND PACK, OR00594K, Item Number 800243011; ortho surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0281-2023·2022-11-30

    Medical device recall: VS3 Iridium infrared fluorescence microscope

    Visionsense, Ltd. issued a voluntary Class II recall of the VS3 Iridium infrared fluorescence microscope affecting 34 units with US Nationwide distribution.

    Product
    VS3 Iridium - Visionsense Infrared (IR) Fluorescence Miniature Microscope (MMS) - 785nm Product Number: 175-0012
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0284-2023·2022-11-30

    Surgical convenience kits recalled for containing recalled 3M drapes

    Orthopedic surgical convenience kits distributed in four states were recalled because they contain 3M surgical drapes that were subject to a separate recall.

    Product
    regard FOOT PACK, OR00123Y, Item Number 880118; orthopedic surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0289-2023·2022-11-30

    Surgical convenience kits recalled due to included 3M surgical drapes

    Surgical convenience kits are being recalled because they contain 3M surgical drapes that were previously recalled. A total of 164 units were distributed to healthcare facilities in Louisiana, Missouri, North Carolina, and Florida.

    Product
    regard SPINE PACK, NU00260H, Item Number 800022008; ortho surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0305-2023·2022-11-30

    Surgical Convenience Kits Recalled by ROi CPS Due to Included 3M Surgical Drapes

    ROi CPS LLC is recalling 456 surgical convenience kits containing 3M surgical drapes that were subject to a separate recall. The kits were distributed across Louisiana, Missouri, North Carolina, and Florida.

    Product
    ¿regard SHOULDER ARTHROSCOPY, OR00049Q, Item Number 880044017; ortho surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0295-2023·2022-11-30

    Recall of Surgical Convenience Kits Containing Recalled 3M Drapes

    ROi CPS LLC is recalling 258 surgical convenience kits containing 3M surgical drapes that were subject to a subsequent recall. The kits were distributed in Louisiana, Missouri, North Carolina, and Florida.

    Product
    regard SPINE PACK,NU00395J, Item Number 800241010; ortho surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0269-2023·2022-11-30

    MicroScan autoSCAN-4 Instrument Recall Due to Incorrect Diffuser Plate

    Beckman Coulter is recalling MicroScan autoSCAN-4 Instruments due to manufacturing with an incorrect diffuser plate component. Affected units were distributed worldwide including multiple U.S. states and countries.

    Product
    MicroScan autoSCAN-4 Instrument, Catalog Number B1018-280
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0310-2023·2022-11-30

    Surgical Convenience Kits Recalled for Included 3M Surgical Drapes

    ROi CPS LLC is recalling 228 gastric surgery convenience kits because they contained 3M surgical drapes that were subsequently recalled. The affected kits were distributed in LA, MO, NC, and FL.

    Product
    regard DAVINCI PACK, GS00137W, Item Number 880132023; gastric surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states