Stryker INFINITY Resect Guide for INBONE Talus — Class II medical device recall Z-1291-2022
Ongoing recall by Wright Medical Technology, Inc., reported 2022-07-06, distributed nationwide. The instrument is incorrectly color coded.
| Recall number | Z-1291-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wright Medical Technology, Inc., Memphis, TN, United States |
| Recall initiated | 2022-06-02 |
| Classified | 2022-06-27 |
| Reported by FDA | 2022-07-06 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BE, CA, CH, DE, FR, GB, HK, IL, SE |
| Quantity | 35 units |
| UPC / GTIN / UDI-DI | 00889797006552 |
| Lot numbers | 2039558 |
| Model numbers | 33620254 |
Product
Stryker INFINITY Resect Guide for INBONE Talus, Size 4, Model #33620254, non-sterile, an instrument used with the INFINITY Total Ankle System.
Reason for recall
The instrument is incorrectly color coded.
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-1291-2022. 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.