Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone — Class II medical device recall Z-1567-2022
Ongoing recall by Wright Medical Technology, Inc., reported 2022-08-31, distributed nationwide. An incorrect sizing label was applied to the carton packaging.
| Recall number | Z-1567-2022 |
|---|---|
| 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 | 2022-07-27 |
| Classified | 2022-08-23 |
| Reported by FDA | 2022-08-31 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, FR, GB, NL, SE |
| Quantity | 17 devices |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00840420121707 |
| Lot numbers | 1728375, 1728376 |
| Model numbers | 4700020 |
Product
Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile.
Reason for recall
An incorrect sizing label was applied to the carton 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-1567-2022. 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.