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B Braun Medical Recalls
444 recalls on record · July 25, 2012 to June 10, 2026 · Drugs, Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
December 30, 2020Medical DevicesFDA
B Braun Medical, Inc. recalls APEX Compounding System Control Panel Module, REF: 601238, Product Code AX1000 - Product Usage: intended for intravascul
Hazard: There is the potential for the compounding system to not immediately interrupt compounding and alert user to the presence of an air bubble exceeding 3% of the ordered volume for an ingredient. This could result in a a compounded drug that does not meet the specified accuracy range for an individual ingredient.
December 30, 2020Medical DevicesFDA
B Braun Medical, Inc. recalls APEX Compounding System Control Panel Module, REF: 601237, Product Code AX1000 - Product Usage: intended for intravascul
Hazard: There is the potential for the compounding system to not immediately interrupt compounding and alert user to the presence of an air bubble exceeding 3% of the ordered volume for an ingredient. This could result in a a compounded drug that does not meet the specified accuracy range for an individual ingredient.
December 30, 2020Medical DevicesFDA
B Braun Medical, Inc. recalls APEX Compounding System Control Panel Module, REF: 601224, Product Code AX1000 - Product Usage: intended for intravascul
Hazard: There is the potential for the compounding system to not immediately interrupt compounding and alert user to the presence of an air bubble exceeding 3% of the ordered volume for an ingredient. This could result in a a compounded drug that does not meet the specified accuracy range for an individual ingredient.
May 6, 2020DrugsFDA
B. Braun Medical Inc recalls Ceftazidime for Injection USP and Dextrose for Injection USP, 2 g, 50 mL Duplex Container, RX only, B Braun Medical Inc.
Hazard: Failed Stability Specifications: Out-of-Specification (OOS) results for High Molecular Weight Polymers.
February 12, 2020Medical DevicesFDA
B. Braun Medical, Inc. recalls Safeline Y-Type Blood Set, Catalog Number V2500
Hazard: Potential for leakage at the joint between the blood filters and tubing
February 12, 2020Medical DevicesFDA
B. Braun Medical, Inc. recalls Safeline Y-Type Blood Set, Catalog Number NF5140
Hazard: Potential for leakage at the joint between the blood filters and tubing
February 12, 2020Medical DevicesFDA
B. Braun Medical, Inc. recalls Y-Type Blood Set, Catalog Number 490530
Hazard: Potential for leakage at the joint between the blood filters and tubing
February 12, 2020Medical DevicesFDA
B. Braun Medical, Inc. recalls Y-Type Blood Set, Catalog Number 490425
Hazard: Potential for leakage at the joint between the blood filters and tubing
February 12, 2020Medical DevicesFDA
B. Braun Medical, Inc. recalls Y-Type Blood Set, Catalog Number 490314
Hazard: Potential for leakage at the joint between the blood filters and tubing
February 12, 2020Medical DevicesFDA
B. Braun Medical, Inc. recalls Y-Type Blood Set, Catalog Number 490293
Hazard: Potential for leakage at the joint between the blood filters and tubing
February 12, 2020Medical DevicesFDA
B. Braun Medical, Inc. recalls Outlook Safety Infusion System Y-type Blood Set, Catalog Number 477005
Hazard: Potential for leakage at the joint between the blood filters and tubing
October 2, 2019Medical DevicesFDA
B. Braun Medical, Inc. recalls B.Braun Infusomat Space Volumetric Infusion Pump Administration Set, Catalog Number 363032
Hazard: Potential for the Infusion Pump Administration Set to leak and/or disconnect at the bonded joint between the tubing and Injection Site (Y-Site).
September 11, 2019Medical DevicesFDA
B. Braun Medical, Inc. recalls CE18TKSTN CONT EPID W/SOFT TIP NRFIT Catalog # 339191
Hazard: The filter capacity is not achieved due to damage of the filter membrane.
September 11, 2019Medical DevicesFDA
B. Braun Medical, Inc. recalls CE18HKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339189
Hazard: The filter capacity is not achieved due to damage of the filter membrane.
September 11, 2019Medical DevicesFDA
B. Braun Medical, Inc. recalls CE18TKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339188
Hazard: The filter capacity is not achieved due to damage of the filter membrane.
September 11, 2019Medical DevicesFDA
B. Braun Medical, Inc. recalls CE17TKFCSN CON EPI TRAY W/17G TUHY NRFIT Catalog # 339187
Hazard: The filter capacity is not achieved due to damage of the filter membrane.
September 11, 2019Medical DevicesFDA
B. Braun Medical, Inc. recalls CE17TKFCN EPID TRAY W/ 17GA TUOHY NRFIT Catalog # 339186
Hazard: The filter capacity is not achieved due to damage of the filter membrane.
September 11, 2019Medical DevicesFDA
B. Braun Medical, Inc. recalls CE17TKN CONT EPIDURALTUOHY NRFIT Catalog # 339183
Hazard: The filter capacity is not achieved due to damage of the filter membrane.
September 11, 2019Medical DevicesFDA
B. Braun Medical, Inc. recalls FEF 100N FLAT EPIDURAL FILTER NRFIT Catalog # 339160
Hazard: The filter capacity is not achieved due to damage of the filter membrane.
September 11, 2019Medical DevicesFDA
B. Braun Medical, Inc. recalls ES1827KN SPINAL/EPIDURAL TRAY NRFIT Catalog # 339115
Hazard: The filter capacity is not achieved due to damage of the filter membrane.
September 11, 2019Medical DevicesFDA
B. Braun Medical, Inc. recalls ES1725KFXN ESPOCAN SPINAL/EPID TRY NRFIT Catalog # 339114
Hazard: The filter capacity is not achieved due to damage of the filter membrane.
June 19, 2019DrugsFDA
B. Braun Medical Inc recalls Heparin Sodium 25,000 USP units per 250 mL (100 USP units per mL) in 5% Dextrose Injection, 250 mL EXCEL Container bag,
Hazard: Subpotent Drug: low out-of-specification results were identified for the drug anti-factor IIa potency which is intended to ensure that the potency of heparin is within the USP specifications.
October 10, 2018Medical DevicesFDA
B. Braun Medical, Inc. recalls BULK NONSTERILE PERIFIX CATHETER CONN., Material Number 8451699N Connection device used by physicians to provide var
Hazard: The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
October 10, 2018Medical DevicesFDA
B. Braun Medical, Inc. recalls DESIGN OPTIONS¿ PAIN MANAGEMENT TRAY, Material Numbers 530029, 530029, 530031, 530035, 530041, 530048, 530068, 530071, 5
Hazard: The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
October 10, 2018Medical DevicesFDA
B. Braun Medical, Inc. recalls EPID. CATH. NG, 20GA. CLOSED TIP-LF, Material Number 333541 Connection device used by physicians to provide various
Hazard: The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
October 10, 2018Medical DevicesFDA
B. Braun Medical, Inc. recalls EC20C 20G X 100CM CATH CLOSED, Material Number 333540 Connection device used by physicians to provide various anesth
Hazard: The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
October 10, 2018Medical DevicesFDA
B. Braun Medical, Inc. recalls EC20CS EPIDURAL CATHETER, Material Number 333532 Connection device used by physicians to provide various anesthetic
Hazard: The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
October 10, 2018Medical DevicesFDA
B. Braun Medical, Inc. recalls EC20CST 20G CLSD SOFT TIP CATH, Material Number 333521 Connection device used by physicians to provide various anest
Hazard: The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
October 10, 2018Medical DevicesFDA
B. Braun Medical, Inc. recalls EC20O 20G X 100CM CATH OPEN TIP LF, Material Number 333520 Connection device used by physicians to provide various a
Hazard: The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
October 10, 2018Medical DevicesFDA
B. Braun Medical, Inc. recalls EC19OF SPRINGWOUND 19G EPID CATHETER, Material Number 333514 Connection device used by physicians to provide various
Hazard: The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.