Stryker CLAW II ORTHOLOC 3DSi Plate — Class II medical device recall Z-0392-2022
Ongoing recall by Wright Medical Technology Inc, reported 2021-12-29, distributed in AZ, IA, ID, NC, NY, VA, WV. The incorrect product is contained in the packaging.
| Recall number | Z-0392-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wright Medical Technology Inc, Arlington, TN, United States |
| Recall initiated | 2021-12-03 |
| Classified | 2021-12-17 |
| Reported by FDA | 2021-12-29 |
| Distributed | AZ, IA, ID, NC, NY, VA, WV |
| Countries outside the US | CA, DE, FR, GB, LB, NL, SA |
| Quantity | 23 units |
| Lot numbers | 1642103 |
| Model numbers | 40240430 |
Product
Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.
Reason for recall
The incorrect product is contained in the packaging.
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-0392-2022. 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.