PERIFIX FX Continuous Epidural Anesthesia Tray — Class II medical device recall Z-0120-2026
Ongoing recall by B BRAUN MEDICAL INC, reported 2025-10-15, distributed nationwide. Potential for the lid of the catheter connector to be in the incorrect position.
| Recall number | Z-0120-2026 |
|---|---|
| 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 | 2025-09-18 |
| Classified | 2025-10-09 |
| Reported by FDA | 2025-10-15 |
| Distributed | Nationwide (US) |
| Quantity | 2,760 units |
| UPC / GTIN / UDI-DI | 04046955901067, 04046955901074 |
| Lot numbers | 0062009622, 0062014350 |
| Model numbers | 332098 |
| Expiration dates | 2026-07-31 |
Product
PERIFIX FX Continuous Epidural Anesthesia Tray, PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle - Winged and 19 Ga. Open tip PERIFIX FX Springwound Epidural Catheter. Product Code: CE17TKFS. Product Description: CE17TKFS EPIDURAL TRAY.
Reason for recall
Potential for the lid of the catheter connector to be in the incorrect position.
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-0120-2026. 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.