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Wishbone Medical, Inc. recalls WishFIX Growth Control Plating System, Model Number: TEFCS28-080US. Orthopedic device.
Recalled May 22, 2024 · FDA recall Z-1808-2024 · Wishbone Medical
Hazard
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. · FDA Class II
Units
60 units
Sold at
US distribution to Florida, New Jersey and Connecticut.
Description
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.
Product
WishFIX Growth Control Plating System, Model Number: TEFCS28-080US. Orthopedic device.
Manufacturer(s)
Wishbone Medical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →