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

14951–14975 of 27471

  • HighFDA (Devices)·Z-0038-2020·2019-10-16

    Vital Scientific V-Twin Automated Chemistry Analyzer Recall for Cooling Defect

    Vital Scientific N.V. is recalling 192 V-Twin automated chemistry analyzers because an improperly installed cooling indicator board may prevent warning signals if reagent cooling fails.

    Product
    V-Twin, Catalog # 6002-800, UDI: 03661540600180 - Product Usage: An in vitro diagnostic device, which is an automated chemistry analyzer, micro type, intended for clinical use in conjunction with certain materials to measure a variety of analytes, including applications in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0101-2020·2019-10-16

    Centurion Medical Recalls VANTEX CVC Bundles Due to Connector Defect

    Centurion Medical Products is recalling VANTEX 7FR, 16CM, 3L CVC Bundles because the included BD MaxZeroNeedleess Connector may leak fluid droplets after disconnection.

    Product
    VANTEX 7FR, 16CM, 3L CVC BUNDLE ECVC6670
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0073-2020·2019-10-16

    BD FACSLyric Flow Cytometer Recall for Potential False High Absolute Counts

    Becton, Dickinson and Company is recalling 236 BD FACSLyric Flow Cytometers because they may produce falsely high absolute counts when used with BD Trucount Tubes.

    Product
    BD FACSLyric Flow Cytometer,3-Laser 10 Color Instrument, REF: 659180 and 65918001, when using BD Trucount Tubes
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-0093-2020·2019-10-16

    Centurion Medical CVC Bundle Recall Due to Fluid Droplet Risk

    Centurion Medical is recalling CVC Bundle Multimeds containing a recalled BD connector due to potential fluid droplet separation.

    Product
    CVC BUNDLE MULTIMED, 3L, 20CM ECVC6060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0089-2020·2019-10-16

    Centurion Medical Recalls Central Venous Access Device Bundles

    Centurion Medical Products Corporation is recalling Central Venous Access Device Bundles because they include a connector recalled for potential fluid droplet separation.

    Product
    CENTRAL VENOUS ACCESS DEVICE BUNDLE ECVC2840
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0102-2020·2019-10-16

    Centurion IV Start Kits Recalled Due to Fluid Droplet Risk

    Centurion Medical Products is recalling IV Start Kits containing a recalled BD connector due to potential fluid droplet separation.

    Product
    IV START KIT IV8440
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0043-2020·2019-10-16

    Roche Online TDM Vancomycin Gen.3 Recalled for Inaccurate Low Sample Results

    Roche Diagnostics is recalling Online TDM Vancomycin Gen.3 kits because they may produce inaccurately low sample results.

    Product
    Online TDM Vancomycin Gen.3 ( 200 tests) Catalog # 06779344190 Analyzer/Module: cobas c 311 and cobas c 501/502
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Devices)·Z-0069-2020·2019-10-16

    BD FACSLyric Flow Cytometer Recall for Potential False High Counts

    Becton, Dickinson and Company is recalling 78 BD FACSLyric Flow Cytometers because they may produce falsely high absolute counts when used with specific tubes, potentially affecting clinical decisions.

    Product
    BD FACSLyric Flow Cytometer, 3-Laser 10 Color Instrument, REF: 662878, and 66287808 when using BD Trucount Tubes
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-0057-2020·2019-10-16

    BD Microtainer Tubes Recalled for Damaged Reservoirs Causing Test Errors

    Becton Dickinson is recalling BD Microtainer Tubes with K2E because damaged reservoirs may cause insufficient sample volume and erroneous test results.

    Product
    BD MicrotainerTubes with K2E (K2EDTA) Catalog Number: 365974
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0075-2020·2019-10-16

    Centurion PICC Line Accessory Kit Recalled for Fluid Droplet Risk

    Centurion Medical Products is recalling PICC Line Accessory Kits containing a BD connector that may release fluid droplets upon disconnection.

    Product
    PICC Line Accessory Kit CVI4285
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0104-2020·2019-10-16

    Centurion Medical Recalls Sorbaview IV Kits Due to Fluid Droplet Risk

    Centurion Medical Products Corporation is recalling Sorbaview IV kits because the included BD MaxZeroNeedleess Connector may release fluid droplets after disconnection.

    Product
    IV KIT - SORBAVIEW IVS3475
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0055-2020·2019-10-16

    BD Microtainer Tubes Recalled for Damaged Reservoirs and Erroneous Test Results

    Becton Dickinson is recalling specific lots of BD Microtainer Tubes with Lithium Heparin because damaged reservoirs may cause insufficient sample volumes and erroneous test results.

    Product
    BD Microtainer Tubes with LH (Lithium Heparin) Part/Catalog No.365965
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0120-2020·2019-10-16

    Centurion Circlamp Recalled for Angle Mismatch Defect

    Centurion Medical Products is recalling 1,530 Circlamps due to a design mismatch that may cause the device to remove foreskin without a scalpel.

    Product
    Centurion CIRCLAMP W/1.1CM BELL - single-use, disposable instrument used to compress the foreskin of the penis during circumcision of a male infant. ReOrder: 310CR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0071-2020·2019-10-16

    BD FACSLyric Flow Cytometer Recall for Potential Inaccurate Cell Counts

    BD Biosciences is recalling 36 BD FACSLyric Flow Cytometers because they may produce falsely high absolute cell counts when used with BD Trucount Tubes, potentially affecting clinical decisions.

    Product
    BD FACSLyric Flow Cytometer, 2-Laser 6 Color Instrument, REF: 651165, when using BD Trucount Tubes
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-0090-2020·2019-10-16

    Centurion Medical CVC Bundle Recall Due to Fluid Droplet Risk

    Centurion Medical Products is recalling CVC Bundles because the included BD MaxZeroNeedleess Connector may release fluid droplets after disconnection.

    Product
    CVC BUNDLE, 20CM, 4L, PI ECVC5095
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0085-2020·2019-10-16

    Centurion Medical Recalls Infusa Port Kits Due to Fluid Droplet Risk

    Centurion Medical Products Corporation is recalling Infusa Port Kits containing a specific connector due to the potential for fluid droplets to separate from the sealed surface.

    Product
    INFUSA PORT KIT DYNDC1840F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0088-2020·2019-10-16

    Centurion Triple Lumen Bundle Kit Recalled for Fluid Droplet Risk

    Centurion Medical Products is recalling Triple Lumen Bundle Kits because the included BD MaxZeroNeedleess Connector may release fluid droplets after disconnection.

    Product
    TRIPLE LUMEN BUNDLE KIT ECVC1540
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0083-2020·2019-10-16

    Centurion Medical Products Recalls CAP CHANGE KIT DYNDC1496B

    Centurion Medical Products is recalling CAP CHANGE KIT DYNDC1496B because the included BD MaxZeroNeedleess Connector may release fluid droplets after disconnection.

    Product
    CAP CHANGE KIT DYNDC1496B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0044-2020·2019-10-16

    Roche AssayTip/AssayCup Tray Recall for Abnormal Internal Structure

    Roche Diagnostics is recalling AssayTip/AssayCup Trays used on the cobas e 801 module due to abnormal internal structure that may lead to incorrect patient results.

    Product
    AssayTip/AssayCup Tray-used on the cobas e 801 module which is a part of the cobas c 8000 MODULAR Analyzer Series (IVD for in vitro determination of analytes in human body fluids) Catalog Number: 5694302001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0103-2020·2019-10-16

    Centurion IV Securement Kit Recall Due to Fluid Droplet Risk

    Centurion Medical Products is recalling IV Securement Kits containing a recalled BD connector due to the potential for fluid droplets to separate from the sealed surface.

    Product
    IV SECUREMENT KIT IVS3405
    Category
    Medical Device
    Distribution
    Distributed nationwide