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

Agency

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

22176–22200 of 40339

  • HighFDA (Devices)·Z-3316-2018·2018-10-10

    B. Braun Medical Recalls Contiplex Tuohy Ultra Catheter Connectors

    B. Braun Medical is recalling 168 Contiplex Tuohy Ultra 2-in-1 connector sets because the connectors may not stay closed, leading to leakage or disconnection.

    Product
    CONTIPLEX TUOHY ULTRA 2 IN CONT. PNB SET, Material Number 331673 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3280-2018·2018-10-10

    Ortho-Clinical VITROS Sodium Slides Recalled for Potential Positively Biased Results

    Ortho-Clinical Diagnostics is recalling VITROS Sodium Slides due to a potential for positively biased results. The recall covers multiple generations and expiry dates distributed globally.

    Product
    VITROS Sodium Slides, Catalog # 837 9034
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3361-2018·2018-10-10

    B. Braun Medical Recalls CE18TBLS Epidural Tray Connectors

    B. Braun Medical is recalling CE18TBLS epidural tray connectors because they may not stay closed, leading to leakage or disconnection.

    Product
    CE18TBLS CONT EPIDURAL TRAY, Material Number 332219 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3362-2018·2018-10-10

    B. Braun Medical Recalls ACCU-BLOC PERIFIX Kits Due to Leakage

    B. Braun Medical is recalling CE18TK ACCU-BLOC PERIFIX Kits because the catheter connectors may not stay closed, causing leakage or disconnection.

    Product
    CE18TK ACCU-BLOC PERIFIX KIT, Material Number 332220 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3379-2018·2018-10-10

    B. Braun Perifix One Epidural Full Tray Recall for Connector Issues

    B. Braun Medical is recalling Perifix One Epidural Full Trays because the catheter connectors may not stay closed, leading to leakage or disconnection.

    Product
    CE18TKO PERIFIX ONE EPIDURAL FULL TRAY, Material Number 332282 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0070-2019·2018-10-10

    Coviden EEA Circular Stapler Recalled for Potential Tissue Gap Defect

    Coviden is recalling 1,902 EEA Circular Staplers with Tri-Staple Technology due to a potential defect that may cause incomplete staple formation or device retention in tissue.

    Product
    EEA Circular Stapler with Tri-Staple Technology, Part No. TRIEEA28MT TRIEEA28XT TRIEEA31MT TRIEEA31XT Product Usage: The EEA Circular Stapler with Tri-Staple Technology places a circular, triple staggered row of titanium staples and resects the excess tissue, creating a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3318-2018·2018-10-10

    B. Braun Medical Recalls Contiplex Tuohy Ultra Catheter Connectors

    B. Braun Medical is recalling Contiplex Tuohy Ultra catheter connectors because they may not stay closed, leading to leakage or disconnection.

    Product
    CONTIPLEX TUOHY ULTRA 4 IN CNB400TU, LF, Material Number 331691 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3342-2018·2018-10-10

    B. Braun Medical Recalls 17 GA Epidural Catheter Connectors

    B. Braun Medical is recalling specific epidural catheter connectors that may not stay closed, leading to potential leakage or disconnection.

    Product
    CE17TKFMHDT 17 GA X 4 FULL EPID KIT, Material Number 332096 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3380-2018·2018-10-10

    B. Braun Recalls 2800 Clamp Style Catheter Connectors Due to Leakage

    B. Braun Medical is recalling 2,800 clamp style catheter connectors because they may not stay closed, leading to leakage or disconnection.

    Product
    CLAMP STYLE CATHETER CONNECTOR 20GA- LF, Material Number 332283 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3355-2018·2018-10-10

    B. Braun Medical Recalls CE18H Continuous Epidural Sets

    B. Braun Medical is recalling CE18H Continuous Epidural Sets because the catheter connectors may not stay closed, potentially causing leakage or disconnection.

    Product
    CE18H CONT EPIDURAL SET, Material Number 332210 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3333-2018·2018-10-10

    B. Braun Recalls Epidural Trays Due to Catheter Connector Leakage

    B. Braun Medical is recalling CE17TKFC Epidural Trays because the catheter connectors may not stay closed, leading to leakage or disconnection.

    Product
    CE17TKFC EPIDURAL TRAY W/ 17GA TUOHY, Material Number 332079 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3390-2018·2018-10-10

    B. Braun Medical Recalls ESPOCAN Combined 27GA Catheter Connectors

    B. Braun Medical is recalling ESPOCAN Combined 27GA catheter connectors because they may not stay closed, leading to leakage or disconnection.

    Product
    ES1827QK ESPOCAN COMBINED 27GA, Material Number 333182 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3326-2018·2018-10-10

    B. Braun Medical Recalls Catheter Connectors Due to Leakage and Disconnection

    B. Braun Medical is recalling 120 catheter connector kits because they may not stay closed, leading to leakage or disconnection.

    Product
    CONT STIM BASIC KIT W/2 IN INSUL TUOHY, Material Number 331757 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3315-2018·2018-10-10

    B. Braun Contiplex Cont Nerve Block Connectors Recalled for Leakage

    B. Braun Medical is recalling Contiplex Cont Nerve Block connectors because they may not stay closed, leading to leakage or disconnection.

    Product
    CNBFX350C CONTIPLEX CONT NERVE BLOCK, Material Number 331672 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3345-2018·2018-10-10

    B. Braun Medical Recalls CNB200TKU Non-Stim Catheter Full Kits

    B. Braun Medical is recalling 880 units of CNB200TKU Non-Stim Catheter Full Kits because the connectors may not stay closed, leading to leakage or disconnection.

    Product
    CNB200TKU NON-STIM CATH FULL KIT, Material Number 332127 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3317-2018·2018-10-10

    B. Braun Medical Recalls Contiplex Tuohy Sets Due to Leakage

    B. Braun Medical is recalling 5,460 units of CNB200T Contiplex Tuohy Sets because the catheter connectors may not stay closed, leading to leakage or disconnection.

    Product
    CNB200T CONTIPLEX TUOHY SET 2 IN, Material Number 331691 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0016-2019·2018-10-10

    Kerlix Bandage Roll Recalled for Potential Sterility Breach

    COVIDIEN LLC is recalling Kerlix Bandage Rolls due to a potential seal defect that could compromise product sterility.

    Product
    Kerlix Bandage Roll, 100 Cotton, 8 Ply, Large 4-1/2 x 9.3 (11.4 cm x 2.8 m), REF 6716 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3398-2018·2018-10-10

    B. Braun Medical Recalls EC19OF Springwound 19G Epidural Catheter Connectors

    B. Braun Medical is recalling EC19OF Springwound 19G epidural catheter connectors because they may not stay closed, leading to leakage or disconnection.

    Product
    EC19OF SPRINGWOUND 19G EPID CATHETER, Material Number 333514 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0013-2019·2018-10-10

    Kerlix AMD Antimicrobial Bandage Roll Recalled for Sterility Breach Risk

    Coviden LLC is recalling Kerlix AMD Antimicrobial Bandage Rolls due to a potential seal defect that could compromise product sterility.

    Product
    Kerlix AMD Antimicrobial Bandage Roll, 6 Ply, 4-1/2 x 12.3 (11.4 cm x 3.7m), REF 3332 Product Usage- as both primary and secondary dressing containing PHMB (polyhexamethylene biguanide) to resist bacterial colonization within the dressing and bacterial penetration through the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3337-2018·2018-10-10

    B. Braun Medical Recalls CE18HKST Catheter Connectors Due to Leakage

    B. Braun Medical is recalling CE18HKST epidural catheter connectors because they may not stay closed, leading to leakage or disconnection.

    Product
    CE18HKST CONT EPID 20G SOFTIP, Material Number 332084 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0063-2019·2018-10-10

    Hemotherm 400CE Recalled for Control Panel Switch Errors

    Cincinnati Sub-Zero is recalling 270 Hemotherm 400CE devices due to potential control panel switch errors that may prevent setting changes or cause unintended changes.

    Product
    Hemotherm 400CE, Catalog Numbers 86022 & 86023 The Hemotherm¿ Dual Reservoir Cooler/Heater is used to lower, maintain, or raise the temperature of the water flowing through a Blood Oxygenator/Heat Exchanger that is used to cool or warm blood during cardiopulmonary bypass…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3356-2018·2018-10-10

    B. Braun Medical Recalls CE18TKCD Epidural Catheter Connectors

    B. Braun Medical is recalling CE18TKCD epidural catheter connectors because they may not stay closed, leading to leakage or disconnection.

    Product
    CE18TKCD CONT EPIDURAL TRAY, Material Number 332211 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the…
    Category
    Medical Device
    Distribution
    Distributed nationwide