Z-2002-2023 Class II Ongoing

Recalled by B. Braun Medical, Inc. — Allentown, PA

Recall Details

Product Type
Devices
Report Date
July 5, 2023
Initiation Date
June 5, 2023
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
16,070 units

Product Description

Perifix¿ / Epidural anesthesia kit (10 count carton)

Reason for Recall

Kits were assembled with the incorrect Filter Straw.

Distribution Pattern

US Nationwide distribution.

Code Information

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