Wright Medical Technology — Class II medical device recall Z-0786-2022
Terminated recall by Wright Medical Technology, Inc., reported 2022-03-23. An incorrect screw is packaged in the product, which contains a locking screw instead of a non-locking screw.
| Recall number | Z-0786-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wright Medical Technology, Inc., Memphis, TN, United States |
| Recall initiated | 2022-02-15 |
| Classified | 2022-03-15 |
| Reported by FDA | 2022-03-23 |
| Terminated | 2022-10-05 |
| Countries outside the US | FR |
| Quantity | 1 packages |
| Lot numbers | 73967511638696 |
| Model numbers | 5201120008 |
Product
Wright Medical Technology, Inc. ORTHOLOC Non-Locking Screw 2mm x 8mm, REF 5201120008, non-sterile, a component of the ORTHOLOC 2.0/2.4 Plate System.
Reason for recall
An incorrect screw is packaged in the product, which contains a locking screw instead of a non-locking screw.
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-0786-2022. 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.