Z-2003-2023 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
3,560 units

Product Description

Design Options¿ / 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. 552177, 552155, 552179, 552116; GTIN: 04046955596102, 04046955214440, 04046955596140, 04046964950254; Lot No. 0061853751, 0061854949, 0061855598, 0061855133.