Vision RingLoc Shell 50 mm Size 23 — Class II medical device recall Z-2483-2015
Terminated recall by Biomet, Inc., reported 2015-09-09. The device was assembled without screw hole plugs.
| Recall number | Z-2483-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2015-07-28 |
| Classified | 2015-08-29 |
| Reported by FDA | 2015-09-09 |
| Terminated | 2016-05-17 |
| Countries outside the US | CA, JP |
| Quantity | 5 |
| Lot numbers | 946410 |
| Model numbers | 135250 |
Product
Vision RingLoc Shell 50 mm Size 23. Hip joint replacement prosthesis.
Reason for recall
The device was assembled without screw hole plugs.
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-2483-2015. 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.