FDA Device recall Z-1917-2024
Centurion OB INSTRUMENT TRAY, REF MN3925
- FDA Device
- Class II
- ongoing
- Published 2024-06-05
On 2024-06-05 the FDA classified a Class II recall of Centurion OB INSTRUMENT TRAY, REF MN3925 by Medline Industries Northfield, citing trumpet Needle Guide ring can detach when excessive pressure is applied.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1917-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-03-01 |
| Published | 2024-06-05 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medline Industries Northfield |
| Distribution | US |
Product
Centurion OB INSTRUMENT TRAY, REF MN3925; Medical procedure convenience tray
Reason
Trumpet Needle Guide ring can detach when excessive pressure is applied.
Identifiers
| code_info | UDI/DI 40653160122945 (case), 10653160122944 (unit), Lot Numbers: 23JBX257, 23KMG455 |
|---|
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-1917-2024%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.