FDA Device recall Z-2627-2023
Perifix¿ / Epidural anesthesia set, medicated
- FDA Device
- Class II
- ongoing
- Published 2023-09-27
On 2023-09-27 the FDA classified a Class II recall of Perifix¿ / Epidural anesthesia set, medicated by B Braun Medical, citing product may be mislabeled with an incorrect lid stock label.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2627-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-07-31 |
| Published | 2023-09-27 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | B Braun Medical |
| Distribution | AR, AZ, CA, FL, GA, IL, MA, MO, NC, NJ, PA, TX, WA |
Product
Perifix¿ / Epidural anesthesia set, medicated
Reason
Product may be mislabeled with an incorrect lid stock label.
Identifiers
| code_info | UDI-DI: 04046964178726 Product Code: 332250; Lot Number 0061863524, expiration date 30.APR.2025 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2627-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.