WishFIX Growth Control Plating System, Model Number: TEFCS28-080US. Orthopedic device.
Reported: May 22, 2024 Initiated: April 5, 2024 #Z-1808-2024
Product Description
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.
Details
- Recalling Firm
- Wishbone Medical, Inc.
- Units Affected
- 60 units
- Distribution
- US distribution to Florida, New Jersey and Connecticut.
- Location
- Warsaw, IN
Frequently Asked Questions
What product was recalled? ▼
WishFIX Growth Control Plating System, Model Number: TEFCS28-080US. Orthopedic device.. Recalled by Wishbone Medical, Inc.. Units affected: 60 units.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 22, 2024. Severity: Moderate. Recall number: Z-1808-2024.
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