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.

Filters

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

26–50 of 40175

  • ModerateFDA (Devices)·Z-0083-2027·2026-10-14

    Beckman Coulter Recalls DxC 500i Clinical Analyzer Modules Due to Software Error

    Beckman Coulter is recalling DxC 500i Clinical Analyzer Modules because a software issue can cause test units to revert to defaults without warning, potentially resulting in falsely elevated reported results.

    Product
    DxC 500i Clinical Analyzer Modules: 1. DxC 500 AU Module w/ISE, DxC 500i, Part No. C63522 2. DxC 500 AU Module, DxC 500i, Part No. C63521 3. Access 2 Module, DxC 500i, Part No. C13252
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0097-2027·2026-10-14

    Avid Medical Recalls Open Heart Kits Due to Lubricant Contamination

    Avid Medical is recalling 124 Open Heart CFH kits because they may be contaminated with a lubricant used during manufacturing.

    Product
    PACK OPEN HEART CFH; Model/Item Number (Kit): 1. UFCF004-06, 2. UFCF004-07;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0092-2027·2026-10-14

    Avid Medical Recalls Davinci Trucustom Bundles Due to Lubricant Contamination

    Avid Medical, Inc. is recalling 144 Davinci Trucustom Bundles because they may be contaminated with a lubricant used during manufacturing.

    Product
    DAVINCI TRUCUSTOM BUNDLE; Model/Item Number (Kit): 1. SAMM064-27, 2. SAMM064-28;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0080-2027·2026-10-14

    Limitless Cryo Spa LLC Recalls Glypto Devices for Lack of 510(k) Clearance

    Limitless Cryo Spa LLC is recalling 219 Glypto Devices and Cryo Machines because they lack FDA 510(k) clearance. The recall covers units distributed nationwide.

    Product
    Glypto Device, Glypto Cryo Machine;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0096-2027·2026-10-14

    AVID Medical Recalls Craniotomy Packs Due to Potential Lubricant Contamination

    AVID Medical, Inc. is recalling 10 Craniotomy Packs (Model WRNM035-20) because they may be contaminated with a lubricant used during manufacturing.

    Product
    CRANIOTOMY PACK; Model/Item Number (Kit): WRNM035-20;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0093-2027·2026-10-14

    AVID Medical Recalls GYN Laparoscopy Kits for Potential Lubricant Contamination

    AVID Medical, Inc. is recalling 134 GYN Laparoscopy/Laparotomy kits due to potential contamination with a manufacturing lubricant.

    Product
    GYN LAPAROSCOPY/LAPAROTOMY; Model/Item Number (Kit): 1. WRNM002-15, 2. FBCH108-03;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0076-2027·2026-10-14

    Quantum Ops Recalls ADAPTABLE Beach Chair Surgical Patient Positioners

    Quantum Ops Inc is recalling 266 ADAPTABLE Beach Chair surgical patient positioners due to a manufacturing issue involving inadequate welds in the patient head positioning system.

    Product
    Brand Name: ADAPTABLE Beach Chair Product Name: Beach Chair surgical patient positioner Model/Catalog Number: 804-33-300 (Enovis); 3105-400-030 (Stryker); internal BC-0001 / BC-0220 Software Version: N/A Product Description: Surgical beach-chair positioner that mounts to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0094-2027·2026-10-14

    Avid Medical Recalls Adult Heart Tray Shands Jacks Due to Lubricant Contamination

    Avid Medical, Inc. is recalling 59 units of Adult Heart Tray Shands Jacks (Model SHND419-08) because they may be contaminated with a lubricant used during manufacturing.

    Product
    ADULT HEART TRAY SHANDS JACKS; Model/Item Number (Kit): SHND419-08;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0084-2027·2026-10-14

    Beckman Coulter DxC 500 AU Clinical Chemistry Analyzers Recalled for Software Error

    Beckman Coulter is recalling DxC 500 AU Clinical Chemistry Analyzers due to a software issue that may cause test units to revert to defaults without warning, potentially resulting in falsely elevated reported results.

    Product
    DxC 500 AU Clinical Chemistry Analyzers: 1. AU w/out ISE, Part No. C63519 2. AU w/ISE, Part No. C63520
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0098-2027·2026-10-14

    Avid Medical Recalls Robotic Prostatectomy Packs for Lubricant Contamination

    Avid Medical, Inc. is recalling six Robotic Prostatectomy Packs (NAMC423-11) because they may be contaminated with a manufacturing lubricant.

    Product
    ROBOTIC PROSTATECTOMY PACK; Model/Item Number (Kit): NAMC423-11;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0117-2027·2026-10-14

    LeMaitre TufTex Over-the-Wire Embolectomy Catheter Recalled for Balloon Failure

    LeMaitre Vascular, Inc. is recalling 54 TufTex Over-the-Wire Embolectomy Catheters because the balloon components may fail under pull force.

    Product
    TufTex¿ Over-the-Wire Embolectomy Catheter; Catalog Number: E1651-88;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0104-2027·2026-10-14

    AVID Medical Recalls Major Packs Due to Potential Lubricant Contamination

    AVID Medical, Inc. is recalling 40 Major Packs (Model NIHB0018-11) because they may be contaminated with a lubricant used during manufacturing.

    Product
    MAJOR PACK; Model/Item Number (Kit): NIHB0018-11;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0105-2027·2026-10-14

    AVID Medical Recalls GYN Laparoscopy Packs Due to Lubricant Contamination

    AVID Medical, Inc. is recalling 28 GYN Laparoscopy Packs (Model NAMC436-12) because they may be contaminated with a lubricant used during manufacturing.

    Product
    GYN LAPAROSCOPY PACK; Model/Item Number (Kit): NAMC436-12;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0106-2027·2026-10-14

    AVID Medical Recalls 23 ABD Hysterectomy Kits Due to Lubricant Contamination

    AVID Medical, Inc. is recalling 23 ABD Hysterectomy kits (Model NAMC438-07) because they may be contaminated with a lubricant used during manufacturing.

    Product
    ABD HYSTERECTOMY; Model/Item Number (Kit): NAMC438-07;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0118-2027·2026-10-14

    Steris HexaVue Focus Integration System Recalled for Patient Data Mismatch

    Steris is recalling 58 HexaVue Focus Integration Systems because a software issue may cause incorrect patient information to appear on printed images.

    Product
    HexaVue Focus Integration System, a single, all-in-one system that handles operating room video routing, surgical video integration, and environmental control, Software Version: 2.0.18
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0089-2027·2026-10-14

    Nihon Kohden CNS-6200 Central Nurse Station Recalled for Cybersecurity Vulnerability

    Nihon Kohden America LLC is recalling 808 CNS-6200 Series Central Nurse Stations due to a cybersecurity vulnerability that could disrupt patient monitoring.

    Product
    Product Name: Nihon Kohden CNS-6200 Series Central Nurse Station, Model/Catalog Number: CN-6201 Software Version: software versions: 01-03, 01-04, 01-05, 01-06, 02-10, 02-11, and 02-40 Product Description: The device is intended for use by medical professionals to provide…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0115-2027·2026-10-14

    Mindray cPM Series Patient Monitor Manuals Recalled for Alarm Clarification

    Mindray DS USA, Inc. is recalling cPM Series Patient Monitor operator's manuals because descriptions of physiological alarm functions may be insufficient or require clarification.

    Product
    cPM Series Patient Monitor. Operator's Manual: cPM 8/cPM 12
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0069-2027·2026-10-14

    Medical Action Industries Recalls Urine Clean Catch Kits Due to Labeling Error

    Medical Action Industries is recalling Urinary Clean Catch kits due to an internal data-entry error that resulted in an incorrect expiration date on the label.

    Product
    Generic Name: Kit, Urine, Clean Catch Trade Name: Kit: Urinary Clean Catch 20/cs Model/Catalog Number: 76769 Lot Number: 333606 UDI-DI: 20809160118228 Software Version: N/A
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-0114-2027·2026-10-14

    Mindray Recalls Passport Series Patient Monitor Operator's Manuals

    Mindray DS USA, Inc. is recalling Passport Series Patient Monitor operator's manuals because descriptions of selected physiological alarm functions may be insufficient or require clarification.

    Product
    Passport Series Patient Monitor. Operator's Manuals: 8 / 12 / 12M / 17M / V
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0109-2027·2026-10-14

    Mindray ePM Series Patient Monitor Manuals Recalled for Alarm Clarification

    Mindray DS USA is recalling ePM Series Patient Monitor operator's manuals because descriptions of physiological alarm functions may be insufficient or require clarification.

    Product
    ePM Series Patient Monitor. Patient Monitor Series: ePM 10M/ePM 12M/ePM 12MA/ ePM 15M/ePM 10A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0113-2027·2026-10-14

    Mindray Recalls BeneView T5 and T8 Operator's Manuals for Alarm Clarification

    Mindray DS USA, Inc. is recalling 133 BeneView T5 and T8 operator's manuals because descriptions of physiological alarm functions may be insufficient or require clarification.

    Product
    BeneView Series. Operator's Manuals: T5 / T8
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0112-2027·2026-10-14

    Mindray Panorama and Telemetry Monitoring System Operator's Manuals Recalled

    Mindray DS USA, Inc. is recalling Panorama and Telemetry Monitoring System operator's manuals because descriptions of selected physiological alarm functions may be insufficient or require clarification.

    Product
    Panorama and Telemetry Monitoring System. Operator's Manuals: TMS-6016/Panorama Telepack-608/TMS60 (TD60).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0110-2027·2026-10-14

    Certain Mindray patient monitor manuals need clarification of alarm functions

    Certain operator's manuals for Mindray BeneVision N1 and N-Series patient monitors contain descriptions that may be insufficient or need clarification about selected physiological alarm functions.

    Product
    BeneVision N1 and N-Series Patient Monitor. Patient Monitor: N12/N15/N17/N19/N22.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0111-2027·2026-10-14

    Mindray BeneVision Telemetry Monitor Manuals Recalled for Alarm Clarification

    Mindray DS USA, Inc. is recalling BeneVision Series Telemetry Monitor operator's manuals because descriptions of selected physiological alarm functions may be insufficient or require clarification.

    Product
    BeneVision Series Telemetry Monitor. Operator's Manuals: TM70/TM80
    Category
    Medical Device
    Distribution
    Distributed nationwide