FDA recall Z-2003-2023
B. Braun Medical, Inc. · Class II · device
Product
Design Options¿ / Epidural anesthesia kit (10 count carton)
Reason for recall
Kits were assembled with the incorrect Filter Straw.
Distribution
US Nationwide distribution.
Key facts
- Status
- Ongoing
- Initiation date
- 2023-06-05
- Report date
- 2023-07-05
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Allentown, PA, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2003-2023