B. Braun Medical, Inc.: Medical Device Recall in 2023 - (Recall #: Z-2002-2023)

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:

Perifix¿ / Epidural anesthesia kit (10 count carton)

Product Classification:

Class II

Date Initiated: June 5, 2023

Date Posted: July 5, 2023

Recall Number: Z-2002-2023

Event ID: 92523

Reason for Recall:

Kits were assembled with the incorrect Filter Straw.

Status: Ongoing

Product Quantity: 16,070 units

Code Information:

Model No. 332217, 332097, 332220, 332078; GTIN: 04046964178283, 04046964177361, 04046964177361, 04046964178320, 04046964177200; Lot No. 0061850767, 0061855339, 00618553400061858554, 0061837264.

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated