WishBone Medical Smart Correction Dual Joint Express Struts — Class II medical device recall Z-1102-2023
Ongoing recall by Wishbone Medical, Inc., reported 2023-02-15, distributed nationwide. Firm identified that user may be unable to adjust the length of the Smart Correction Dual Joint Express Struts
| Recall number | Z-1102-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wishbone Medical, Inc., Warsaw, IN, United States |
| Recall initiated | 2023-01-04 |
| Classified | 2023-02-07 |
| Reported by FDA | 2023-02-15 |
| Distributed | Nationwide (US) |
| Quantity | 195 |
| Lot numbers | 1048176, 1048177, 1048178, 1048179, 1048180, 1048221XS, 1048222, 1048223 |
| Model numbers | 10-702-080095-0, 10-702-080095-0XS, 10-702-095115-0, 10-702-115150-0, 10-702-140200, 10-702-190300-0 |
Product
WishBone Medical Smart Correction Dual Joint Express Struts, external skeleton fixation device Type Part Number XXS 10-702-080095-0 XS 10-702-095115-0 Short 10-702-115150-0 Medium 10-702-140200 Long 10-702-190300-0
Reason for recall
Firm identified that user may be unable to adjust the length of the Smart Correction Dual Joint Express Struts due to the collar release pin backing out. This may lead to a delay in correction.
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-1102-2023. 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.