Recall Z-2003-2023— B. Braun Medical, Inc.

Name: FDA recall Z-2003-2023
Creator: U.S. Food and Drug Administration
Published: 2023-06-05

Class II · Ongoing

Class II FDA medical device recall by B. Braun Medical, Inc., initiated 2023-06-05. FDA's recall record names no specific 510(k) clearance for this event. Product: Design Options¿ / Epidural anesthesia kit (10 count carton). Reason: Kits were assembled with the incorrect Filter Straw..

Recalling firm: B. Braun Medical, Inc.
Classification: Class II
Status: Ongoing
Initiated: 2023-06-05
Firm location: Allentown, PA, United States

Product description

Design Options¿ / Epidural anesthesia kit (10 count carton)

Reason for recall

Kits were assembled with the incorrect Filter Straw.

Data sourced from openFDA. This site is unofficial and independent of the FDA.