Wishbone Medical, Inc. recalls WishFIX Growth Control Plating System, Model Number: TEFCS28-080US. Orthopedic device.
- Recall date
- April 5, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1808-2024
- FDA classification
- Class II
- Brand / firm
- Wishbone Medical, Inc.
- Sold / distributed
- US distribution to Florida, New Jersey and Connecticut.
Why it was recalled
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.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
WishFIX Growth Control Plating System, Model Number: TEFCS28-080US. Orthopedic device.
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