FDA Device recall Z-2483-2015
Vision RingLoc Shell 50 mm Size 23
- FDA Device
- Class II
- terminated
- Published 2015-09-09
On 2015-09-09 the FDA classified a Class II recall of Vision RingLoc Shell 50 mm Size 23 by Biomet, citing the device was assembled without screw hole plugs.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2483-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-07-28 |
| Published | 2015-09-09 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Biomet |
| Distribution | n/a |
Product
Vision RingLoc Shell 50 mm Size 23. Hip joint replacement prosthesis.
Reason
The device was assembled without screw hole plugs.
Identifiers
| code_info | Part Number:135250; Lot Number:946410 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2483-2015%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.