Perifix¿ / Epidural anesthesia set — Class II medical device recall Z-2627-2023
Ongoing recall by B. Braun Medical, Inc., reported 2023-09-27, distributed in AR, AZ, CA, FL, GA, IL, MA, MO…. Product may be mislabeled with an incorrect lid stock label.
| Recall number | Z-2627-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | B. Braun Medical, Inc., Allentown, PA, United States |
| Recall initiated | 2023-07-31 |
| Classified | 2023-09-21 |
| Reported by FDA | 2023-09-27 |
| Distributed | AR, AZ, CA, FL, GA, IL, MA, MO, NC, NJ, PA, TX, WA |
| Quantity | 3,440 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 04046964178726 |
| Lot numbers | 0061863524 |
| Expiration dates | 2025-04-20 |
Product
Perifix¿ / Epidural anesthesia set, medicated
Reason for recall
Product may be mislabeled with an incorrect lid stock label.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2627-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.