FDA Device recall Z-1808-2024
WishFIX Growth Control Plating System, Model Number: TEFCS28-080US. Orthopedic device
- FDA Device
- Class II
- ongoing
- Published 2024-05-22
On 2024-05-22 the FDA classified a Class II recall of WishFIX Growth Control Plating System, Model Number: TEFCS28-080US. Orthopedic device by Wishbone Medical, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1808-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-04-05 |
| Published | 2024-05-22 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Wishbone Medical |
| Distribution | CT, FL, NJ |
Product
WishFIX Growth Control Plating System, Model Number: TEFCS28-080US. Orthopedic device.
Reason
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.
Identifiers
| code_info | Model Number: TEFCS28-08-US; UDI/DI: B562TEFCS2808US0; Lot Number: 28042 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1808-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.