The Recall Desk

Manufacturer

B. Braun Medical, Inc.

446 recalls in our database name B. Braun Medical, Inc. as the manufacturing or recalling firm.

What the numbers show

Total
446
Critical
9
Severe
40
Most recent
2026-09-09

Of the 446 recalls from B. Braun Medical, Inc. we have scored against our rubric, 9 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 40 (9%) are Severe.

Which agencies issued them

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

276–300 of 446

  • SevereFDA (Drugs)·D-1257-2020·2020-05-06

    B. Braun Recalls Ceftazidime and Dextrose Injection Due to Stability Failures

    B. Braun Medical Inc. is recalling one lot of Ceftazidime for Injection USP and Dextrose for Injection USP because the product failed stability specifications for high molecular weight polymers.

    Product
    Ceftazidime for Injection USP and Dextrose for Injection USP, 2 g, 50 mL Duplex Container, RX only, B Braun Medical Inc., Bethlehem, PA 18018-3524, NDC 0264-3145-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0937-2020·2020-02-12

    B. Braun Recalls Y-Type Blood Sets Due to Leakage Risk

    B. Braun Medical is recalling 5,616 Y-Type Blood Sets because of a potential for leakage at the joint between the blood filters and tubing.

    Product
    Y-Type Blood Set, Catalog Number 490314
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0941-2020·2020-02-12

    B. Braun Recalls Safeline Y-Type Blood Sets Due to Leakage Risk

    B. Braun Medical is recalling 19,500 Safeline Y-Type Blood Sets due to a potential for leakage at the joint between the blood filters and tubing.

    Product
    Safeline Y-Type Blood Set, Catalog Number V2500
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0936-2020·2020-02-12

    B. Braun Recalls Y-Type Blood Sets Due to Leakage Risk

    B. Braun Medical is recalling 1,050 Y-Type Blood Sets because they may leak at the joint between the blood filters and tubing.

    Product
    Y-Type Blood Set, Catalog Number 490293
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0938-2020·2020-02-12

    B. Braun Y-Type Blood Set Recall Due to Leakage Risk

    B. Braun Medical is recalling 2,736 Y-Type Blood Sets due to a potential for leakage at the joint between the blood filters and tubing.

    Product
    Y-Type Blood Set, Catalog Number 490425
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0939-2020·2020-02-12

    B. Braun Recalls Y-Type Blood Sets Due to Leakage Risk

    B. Braun Medical is recalling 9,000 Y-Type Blood Sets because of a potential for leakage at the joint between the blood filters and tubing.

    Product
    Y-Type Blood Set, Catalog Number 490530
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0940-2020·2020-02-12

    B. Braun Recalls Safeline Y-Type Blood Sets Due to Leakage Risk

    B. Braun Medical is recalling 3,300 units of Safeline Y-Type Blood Sets due to a potential for leakage at the joint between the blood filters and tubing.

    Product
    Safeline Y-Type Blood Set, Catalog Number NF5140
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0935-2020·2020-02-12

    B. Braun Outlook Safety Infusion System Y-type Blood Set Recall for Leakage

    B. Braun Medical is recalling 1,824 Outlook Safety Infusion System Y-type Blood Sets due to a potential for leakage at the joint between the blood filters and tubing.

    Product
    Outlook Safety Infusion System Y-type Blood Set, Catalog Number 477005
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2489-2019·2019-10-02

    B.Braun Infusion Pump Administration Set Recalled for Potential Leaks

    B. Braun Medical is recalling 2,580 Infusomat Space Volumetric Infusion Pump Administration Sets due to a risk of leaking or disconnecting at the Y-site joint.

    Product
    B.Braun Infusomat Space Volumetric Infusion Pump Administration Set, Catalog Number 363032
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-2466-2019·2019-09-11

    B. Braun Medical Recalls Espocan Spinal/Epidural Trial Needles

    B. Braun Medical is recalling 100 units of Espocan Spinal/Epidural Trial Needles because damage to the filter membrane prevents the filter from achieving its intended capacity.

    Product
    ES1725KFXN ESPOCAN SPINAL/EPID TRY NRFIT Catalog # 339114
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-2469-2019·2019-09-11

    B. Braun Medical Recalls Epidural Tuohy Needle Filters Due to Membrane Damage

    B. Braun Medical is recalling 540 units of CE17TKN epidural Tuohy needle filters because the filter membrane is damaged, preventing the device from achieving its intended filter capacity.

    Product
    CE17TKN CONT EPIDURALTUOHY NRFIT Catalog # 339183
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-2468-2019·2019-09-11

    B. Braun Recalls FEF 100N Flat Epidural Filters Due to Membrane Damage

    B. Braun Medical is recalling 250 units of FEF 100N Flat Epidural Filters because damage to the filter membrane prevents the device from achieving its intended filter capacity.

    Product
    FEF 100N FLAT EPIDURAL FILTER NRFIT Catalog # 339160
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-2473-2019·2019-09-11

    B. Braun Medical Recalls Accu-Bloc Perifix Kits Due to Filter Damage

    B. Braun Medical is recalling 200 units of Accu-Bloc Perifix Kits because damaged filter membranes may prevent the device from achieving required filter capacity.

    Product
    CE18HKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339189
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-2472-2019·2019-09-11

    B. Braun Medical Recalls Accu-Bloc Perifix Kits Due to Filter Damage

    B. Braun Medical is recalling 3,820 units of Accu-Bloc Perifix Kits because damage to the filter membrane prevents the device from achieving its intended filter capacity.

    Product
    CE18TKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339188
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-2471-2019·2019-09-11

    B. Braun Medical Recalls Con Epi Tray Due to Filter Membrane Damage

    B. Braun Medical is recalling 200 units of Con Epi Trays because damage to the filter membrane prevents the device from achieving its required filter capacity.

    Product
    CE17TKFCSN CON EPI TRAY W/17G TUHY NRFIT Catalog # 339187
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-2474-2019·2019-09-11

    B. Braun Medical Recalls Cont. Epidural Needles Due to Filter Damage

    B. Braun Medical is recalling 1,230 units of CE18TKSTN Cont. Epidural Needles because the filter membrane is damaged, preventing the device from achieving its intended filter capacity.

    Product
    CE18TKSTN CONT EPID W/SOFT TIP NRFIT Catalog # 339191
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-2467-2019·2019-09-11

    B. Braun Recalls Spinal and Epidural Trays Due to Filter Damage

    B. Braun Medical is recalling 200 units of spinal and epidural trays because the filter membrane is damaged, preventing the device from achieving required filter capacity.

    Product
    ES1827KN SPINAL/EPIDURAL TRAY NRFIT Catalog # 339115
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-2470-2019·2019-09-11

    B. Braun Epidural Tray Recall Due to Filter Membrane Damage

    B. Braun Medical is recalling 960 epidural trays because filter membrane damage prevents the filter from achieving its intended capacity.

    Product
    CE17TKFCN EPID TRAY W/ 17GA TUOHY NRFIT Catalog # 339186
    Category
    Medical Device
    Distribution
    10 states
  • ModerateFDA (Drugs)·D-1343-2019·2019-06-19

    B. Braun Recalls Heparin Sodium Bags Due to Low Potency

    B. Braun Medical Inc. is recalling 40,176 bags of Heparin Sodium in Dextrose because testing showed the drug had lower potency than required by USP specifications.

    Product
    HEPARIN SODIUM IN DEXTROSE — HEPARIN SODIUM IN DEXTROSE (HEPARIN SODIUM AND DEXTROSE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3364-2018·2018-10-10

    B. Braun Medical Recalls CE18TB Epidural Trays Due to Leakage

    B. Braun Medical is recalling CE18TB epidural trays because the catheter connectors may not stay closed, causing leakage or disconnection.

    Product
    CE18TB CONT EPIDURAL TRAY, Material Number 332222 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 ca
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3321-2018·2018-10-10

    B. Braun Medical Recalls Contiplex Tuohy Sets Due to Leakage

    B. Braun Medical is recalling 1,848 Contiplex Tuohy Sets because the catheter connectors may not stay closed, leading to leakage or disconnection.

    Product
    CONTIPLEX TUOHY SET, 18GX11/2X 1,3X40MM, Material Number 331695 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 conjuncti
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3381-2018·2018-10-10

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

    B. Braun Medical is recalling 6,850 clamp-style catheter connectors because they may not stay closed, causing leakage or disconnection.

    Product
    CLAMP STYLE CATH. CONNECTOR 18-19 GA- LF, Material Number 332285 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 conjunct
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3375-2018·2018-10-10

    B. Braun Medical Recalls Epidural Catheter Connectors Due to Leakage

    B. Braun Medical is recalling 1,980 epidural catheter connectors because they may not stay closed, leading to leakage or disconnection.

    Product
    CE17TB19C CONT EPIDURAL TRAY, Material Number 332242 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-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 t
    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 conjunction
    Category
    Medical Device
    Distribution
    Distributed nationwide

About this company

Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.

B Braun Medical (United States)

company in Bethlehem, United States

Country
United States
Founded
1839

Official website

Source: Wikidata (Q30264023), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.