FDA Device recall Z-0126-2026
Design Options, PERIFIX FX Epidural Anesthesia Tray
- FDA Device
- Class II
- ongoing
- Published 2025-10-15
On 2025-10-15 the FDA classified a Class II recall of Design Options, PERIFIX FX Epidural Anesthesia Tray by B Braun Medical, citing potential for the lid of the catheter connector to be in the incorrect position.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0126-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-09-18 |
| Published | 2025-10-15 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | B Braun Medical |
| Distribution | US |
Product
Design Options, PERIFIX FX Epidural Anesthesia Tray. Product Code: CESK. Product Descriptions: 1. CESK ROBERT WOOD JOHNSON UNIV HOSP. 2. CESK EAST JEFFERSON GEN HOSP 20071769. 3. CESK FLETCHER ALLEN HOSPITAL. 4. CESK WASHOE MEDICAL CENTER. 5. CESK DETROIT MEDICAL CTR 20064586. 6. CESK ALBANY MEDICAL CENTER. 7. CESK EPIDURAL BLOCK TRAY. 8. CESK, BSW EPIDURAL TRAY. 9. CESK HOWARD COUNTY GENERAL. 10. CESK CE17TKFC10L. 11. CESK WILLIAMSON MEDICAL CENTER. 12. CESK FLORIDA HOSPITAL. 13. CESK RIVERSIDE HEALTH SYSTEM. 14. CESK MAYO CLINIC OB. 15. CESK PRESBYTERIAN HOSPITAL DALLAS. 16. CESK HOUSTON METHODIST HOSPITAL. 17. CESK OHIO STATE UNIV MEDICAL CENTER. 18. CESK NORTONS WOMEN'S AND CHILDREN'S. 19. CESK BEN TAUB. 20. CESK PENN MEDICINE CONTINUOUS-ORIG CUST. 21. CESK ALLEGHENY GENERAL HOSPITAL. 22. CESK UNIVERSITY OF ILLINOIS MED CTR. 23. CESK RUSH UNIVERSITY MEDICAL CENTER. 24. CESK ST. JOSEPH MEDICAL CENTER. 25. CESK INTEGRIS HEALTH. 26. CESK UMASS MEMORIAL. 27. CESK STANFORD UNIV HOSP 20054718. 28. CESK OVERLAKE HOSPITAL. 29. CESK CHRIST HOSPITAL 20057985. 30. CESK NEWTON-WELLESLEY HOSPITAL.
Reason
Potential for the lid of the catheter connector to be in the incorrect position.
Identifiers
| code_info | 1. REF: 551028; Product Code: CESK; UDI-DI (Primary): 04046964306334; UDI-DI (Unit of Use): 04046964306327; Lot Number:…1. REF: 551028; Product Code: CESK; UDI-DI (Primary): 04046964306334; UDI-DI (Unit of Use): 04046964306327; Lot Number: 0062017630. 2. REF: 551474; Product Code: CESK; UDI-DI (Primary): 04046964306938; UDI-DI (Unit of Use): 04046964306921; Lot Number: 0062006292. 3. REF: 551630; Product Code: CESK; UDI-DI (Primary): 04046964307560; UDI-DI (Unit of Use): 04046964307546; Lot Number: 0062017605. 4. REF: 551749: Product Code: CESK; UDI-DI (Primary): 04046964307942; UDI-DI (Unit of Use): 04046964307935; Lot Number: 0062017615. 5. REF: 551769: Product Code: CESK; UDI-DI (Primary): 04046964308024; UDI-DI (Unit of Use): 04046964308017; Lot Number: 0062006304. 6. REF: 551998: Product Code: CESK; UDI-DI (Primary): 04046964310942; UDI-DI (Unit of Use): 04046964310928; Lot Number: 0062014368. 7. REF: 552006: Product Code: CESK; UDI-DI (Primary): 04046964311215; UDI-DI (Unit of Use): 04046964311192; Lot Number: 0062013265. 8. REF: 552076: Product Code: CESK; UDI-DI (Primary): 04046964814 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0126-2026%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.