B. Braun Medical, Inc.: Medical Device Recall in 2023 - (Recall #: Z-2003-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: June 5, 2023

Date Posted: July 5, 2023

Recall Number: Z-2003-2023

Event ID: 92523

Reason for Recall:

Kits were assembled with the incorrect Filter Straw.

Status: Ongoing

Product Quantity: 3,560 units

Code Information:

Model No. 552177, 552155, 552179, 552116; GTIN: 04046955596102, 04046955214440, 04046955596140, 04046964950254; Lot No. 0061853751, 0061854949, 0061855598, 0061855133.

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated