Arcos Modular Revision Hip System High Offset Cone Prox Body — Class II medical device recall Z-2266-2021
Terminated recall by Biomet, Inc., reported 2021-08-18, distributed nationwide. Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device
| Recall number | Z-2266-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2021-06-02 |
| Classified | 2021-08-12 |
| Reported by FDA | 2021-08-18 |
| Terminated | 2022-07-06 |
| Distributed | Nationwide (US) |
| Quantity | 7 units |
| UPC / GTIN / UDI-DI | 00880304480551 |
| Model numbers | 11-301315 |
Product
Arcos Modular Revision Hip System High Offset Cone Prox Body, Size E, 60 MM Item Number: 11-301315
Reason for recall
Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention
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-2266-2021. 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.