Recall company profile

B. Braun Medical, Inc. Recalls

Overview of recall records associated with B. Braun Medical, Inc., including dates, categories and classifications where available.

366recall records
Sep 16, 2026latest record date
Jan 22, 2014earliest record date

Recall history in this database

Classification mix: Class II: 335, Class I: 30, Class III: 1.

Medical DeviceJul 31, 2024

Perfusor Space Syringe Pump, Wireless recall — FDA Z-2434-2024

Perfusor Space Syringe Pump's instructions for use previously identified Monoject syringes as an option for use. However, changes to manufacturing to Cardinal Health Monoject syringes may…

Class IIFDA: OngoingB Braun Medical Inc.
Medical DeviceJul 31, 2024

Perfusor PCA Syringe Pump recall — FDA Z-2435-2024

Perfusor Space Syringe Pump's instructions for use previously identified Monoject syringes as an option for use. However, changes to manufacturing to Cardinal Health Monoject syringes may…

Class IIFDA: OngoingB Braun Medical Inc.
Medical DeviceJul 31, 2024

PERFUSOR SPACE ACM-KIT recall — FDA Z-2436-2024

Perfusor Space Syringe Pump's instructions for use previously identified Monoject syringes as an option for use. However, changes to manufacturing to Cardinal Health Monoject syringes may…

Class IIFDA: OngoingB Braun Medical Inc.
Medical DeviceJul 31, 2024

Perfusor Space Infusion Pump System recall — FDA Z-2433-2024

Perfusor Space Syringe Pump's instructions for use previously identified Monoject syringes as an option for use. However, changes to manufacturing to Cardinal Health Monoject syringes may…

Class IIFDA: OngoingB Braun Medical Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies B. Braun Medical, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.