Biomet RingLoc Hip System Self-Tapping Bone Screw 6 — Class II medical device recall Z-1087-2019
Terminated recall by Zimmer Biomet, Inc., reported 2019-04-10, distributed nationwide. Two lengths of the 6.5mm RingLoc Hip System Self-Tapping Bone Screw may have the potential for the 30mm screws
| Recall number | Z-1087-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2019-03-01 |
| Classified | 2019-04-04 |
| Reported by FDA | 2019-04-10 |
| Terminated | 2020-05-27 |
| Distributed | Nationwide (US) |
| Countries outside the US | CL, CN, CR, IN, JP, MX, SG |
| Quantity | 809 units |
| UPC / GTIN / UDI-DI | 00880304008700 |
| Model numbers | 103533 |
Product
Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx30mm-Low Profile Titanium, Accessory to total hip implant Item Number: 103533 Product Usage: Accessory to total hip implant
Reason for recall
Two lengths of the 6.5mm RingLoc Hip System Self-Tapping Bone Screw may have the potential for the 30mm screws to be packaged as 20mm screws and vice versa.
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-1087-2019. 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.