The Recall Desk

State

Oklahoma product recalls

73,741 recalls have nationwide distribution and so reach Oklahoma. 5,822 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total
5,822
Critical
1,040
Severe
1,493
Most recent
2026-10-28

Of the 5,822 recalls naming Oklahoma we have scored against our rubric, 1,040 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,493 (26%) are Severe.

These figures cover only the 5,822 recalls whose distribution notice names Oklahoma specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39601–39625 of 79563

  • HighFDA (Devices)·Z-0065-2019·2018-10-10

    Vision RT AlignRT Plus Integrated Gate Controller PCB Recall

    Vision RT Ltd is recalling 690 AlignRT Plus systems due to an RTInterface error that can occur during I/O communication between the Integrated Gate Controller PCB and the Framegrabber PCB.

    Product
    Integrated Gate Controller PCB (component of AlignRT Plus) Truebeam variant only. The AlignRT is a video-based three-dimensional (3D) surface imaging system which is used to image the skin surface of a patient in 3D before and during radiotherapy treatment. Part number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3319-2018·2018-10-10

    B. Braun Medical Recalls Contiplex Tuohy Sets Due to Leakage

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

    Product
    CONTIPLEX TUOHY SET, 18GX4", 1.3X100MM, Material Number 331693 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-3383-2018·2018-10-10

    B. Braun Medical Recalls Epid Paed Full Kit Catheter Connectors

    B. Braun Medical is recalling 610 units of Epid Paed Full Kit catheter connectors because they may not stay closed, leading to leakage or disconnection.

    Product
    EPID PAED FULL KIT 24GA CT NG CATH LF, Material Number 332292 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-3382-2018·2018-10-10

    B. Braun Recalls Pediatric Epidural Catheter Connectors Due to Leakage

    B. Braun Medical is recalling 1,380 pediatric epidural catheter connectors because they may not stay closed, causing leakage or disconnection.

    Product
    CEP18TKO CONT. EPIDURAL PEDIATRIC KIT, Material Number 332290 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-3376-2018·2018-10-10

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

    B. Braun Medical is recalling 4,150 epidural catheter connectors because they may not stay closed, causing leakage or disconnection.

    Product
    CE17TK19CDP CONT EPIDURAL TRAY, Material Number 332262 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-3389-2018·2018-10-10

    B. Braun Medical Recalls Spinal and Epidural Catheter Connectors

    B. Braun Medical is recalling ES1725K Spinal/Epidural Trays because the catheter connectors may not stay closed, leading to leakage or disconnection.

    Product
    ES1725K SPINAL/EPIDURAL TRAY, Material Number 333165 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-3370-2018·2018-10-10

    B. Braun Medical Recalls CE17TKPS Continuous Epidural Anesthesia Trays

    B. Braun Medical is recalling CE17TKPS Continuous Epidural Anesthesia Trays because the catheter connectors may not stay closed, leading to leakage or disconnection.

    Product
    CE17TKPS CONTINUOUS EPIDURAL ANES TRAY, Material Number 332233 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-0049-2019·2018-10-10

    Oridion Capnostream20 N Monitors Recalled for Settings Reset Issue

    Oridion Medical is recalling five Capnostream20 N bedside monitors because date, time, and alarm settings may reset to factory defaults when powered off.

    Product
    Capnostream20 N W/PRINTER CYVITAL, CS08798
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3385-2018·2018-10-10

    B. Braun Accu-Bloc Perifix Kit Recalled for Catheter Leakage

    B. Braun Medical is recalling 1,380 Accu-Bloc Perifix Kits because the catheter connectors may not stay closed, leading to leakage or disconnection.

    Product
    GOVCE18TK ACCU-BLOC PERIFIX KIT, Material Number 332600 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-3392-2018·2018-10-10

    B. Braun Medical Recalls Espocan Spinal/Epid Trays Due to Leakage

    B. Braun Medical is recalling 1,490 Espocan Spinal/Epid Trays because the catheter connectors may not stay closed, causing leakage or disconnection.

    Product
    ESPOCAN SPINAL/EPID TRAY W/ 18G TUOHY, Material Number 333193 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-0001-2019·2018-10-10

    Smith & Nephew Recalls Journey BCS Knee CoCr Femoral Components

    Smith & Nephew is recalling Journey BCS Knee CoCr Femoral Components because registry data indicates the first-generation system has a revision rate over 1.5 times the class average.

    Product
    Journey BCS Knee CoCr Femoral Components, Catalog Numbers: 74021210, 74021211, 74021212, 74021213, 74021214, 74021215, 74021216, 74021217, 74021218, 74021219, 74021220, 74021221, 74021222, 74021223, 74021224, 74021225, 74021226, 74021227, 74021228, 74021229
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3354-2018·2018-10-10

    B. Braun Medical Recalls CE18HKCD Epidural Tray Connectors

    B. Braun Medical is recalling CE18HKCD epidural tray connectors because they may not stay closed, leading to leakage or disconnection.

    Product
    CE18HKCD CONT EPIDURAL TRAY, Material Number 332206 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-3313-2018·2018-10-10

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

    B. Braun Medical is recalling 600 CONTI TUOHY ULTRA 360 catheter connectors because they may not stay closed, leading to leakage or disconnection.

    Product
    CONTI TUOHY ULTRA 360 2 IN CONT PNB SET, Material Number 331640 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-3360-2018·2018-10-10

    B. Braun Medical Recalls 18GA Tuohy Catheter Connectors for Leakage

    B. Braun Medical is recalling 18GA Tuohy catheter connectors because they may not stay closed, leading to leakage or disconnection.

    Product
    CE18TKCD10L 18GA TUOHY/10CC GLAS, Material Number 332217 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-3391-2018·2018-10-10

    B. Braun Recalls Spinal and Epidural Catheter Connectors Due to Leakage

    B. Braun Medical is recalling ES1827K Spinal/Epidural Trays because the catheter connectors may not stay closed, leading to leakage or disconnection.

    Product
    ES1827K SPINAL/EPIDURAL TRAY (LF), Material Number 333192 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-3349-2018·2018-10-10

    B. Braun Catheter Connectors Recalled for Leakage and Disconnection

    B. Braun Medical is recalling 1,350 CNB400TU3KUE catheter connectors because they may not stay closed, leading to leakage or disconnection.

    Product
    CNB400TU3KUE 18GX4 CONTI THY ULTRA 360, Material Number 332170 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-0020-2019·2018-10-10

    Oridion CAPNOSTREAM 20 Patient Monitors Recalled for Settings Reset

    Oridion Medical is recalling 3,143 CAPNOSTREAM 20 patient monitors because date, time, and alarm settings may reset to factory defaults when powered off.

    Product
    CAPNOSTREAM 20 (US) N, Part Number CS08651
    Category
    Medical Device
    Distribution
    Distributed nationwide