Z-2002-2023 Class II Ongoing
FDA device recall Z-2002-2023 was initiated by B. Braun Medical, Inc. on June 5, 2023 and is designated Class II. Reason for recall: Kits were assembled with the incorrect Filter Straw. The recall status is ongoing. Affected quantity: 16,070 units.
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.