FDA recall Z-2627-2023
B. Braun Medical, Inc. · Class II · device
Product
Perifix¿ / Epidural anesthesia set, medicated
Reason for recall
Product may be mislabeled with an incorrect lid stock label.
Distribution
US Distributions to states of - AR, AZ, CA, FL, GA, IL, MA, MO, NC, NJ, PA, TX, WA
Key facts
- Status
- Ongoing
- Initiation date
- 2023-07-31
- Report date
- 2023-09-27
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Allentown, PA, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2627-2023