ALTERA Spacer ALTERA Spacer — Class II medical device recall Z-2867-2020
Terminated recall by Globus Medical, Inc., reported 2020-09-02. Specific lots of ALTERA¿ implants have internal components that may have been manufactured using stainless ste
| Recall number | Z-2867-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Globus Medical, Inc., Audubon, PA, United States |
| Recall initiated | 2020-07-22 |
| Classified | 2020-08-22 |
| Reported by FDA | 2020-09-02 |
| Terminated | 2021-08-19 |
| UPC / GTIN / UDI-DI | 00889095069891 |
| Model numbers | 1124.1213 |
Product
ALTERA Spacer ALTERA Spacer, 10x36, 10-14mm, 8¿
Reason for recall
Specific lots of ALTERA¿ implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy.
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-2867-2020. 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.