Stryker Infinity Alignment Frame Distal Sub-Assembly — Class II medical device recall Z-2105-2023
Ongoing recall by Wright Medical Technology, Inc., reported 2023-07-12. The devices were manufactured with the pin sleeve holes too narrow, which does not allow the pin sleeves to pa
| Recall number | Z-2105-2023 |
|---|---|
| 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 | 2023-06-13 |
| Classified | 2023-07-06 |
| Reported by FDA | 2023-07-12 |
| Countries outside the US | AU, BE, CA, CH, CL, CN, CO, DE, ES, FR, GB, IT, MX, NL, SE, TW |
| Quantity | 106 devices |
| UPC / GTIN / UDI-DI | 00889797003926 |
| Lot numbers | 2656815, 2762126 |
| Model numbers | 33600020 |
Product
Stryker Infinity Alignment Frame Distal Sub-Assembly, Catalog #33600020, non-sterile.
Reason for recall
The devices were manufactured with the pin sleeve holes too narrow, which does not allow the pin sleeves to pass through the pin sleeve holes, thereby preventing pin placement through the pin holes.
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-2105-2023. 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.