WishFIX Growth Control Plating System — Class II medical device recall Z-1808-2024
Ongoing recall by Wishbone Medical, Inc., reported 2024-05-22, distributed in CT, FL, NJ. The products in this lot are incorrectly packed with a Stainless-Steel implant instead of a Titanium implant a
| Recall number | Z-1808-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wishbone Medical, Inc., Warsaw, IN, United States |
| Recall initiated | 2024-04-05 |
| Classified | 2024-05-10 |
| Reported by FDA | 2024-05-22 |
| Distributed | CT, FL, NJ |
| Quantity | 60 units |
| Lot numbers | 28042 |
| Model numbers | TEFCS28-08-US, TEFCS28-080US |
Product
WishFIX Growth Control Plating System, Model Number: TEFCS28-080US. Orthopedic device.
Reason for recall
The products in this lot are incorrectly packed with a Stainless-Steel implant instead of a Titanium implant as the packaging and part number indicated.
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-1808-2024. 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.