FDA recall record

Wishbone Medical WishFIX Growth Control Plating System recall — FDA Z-1808-2024

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 IIclassification
Z-1808-2024official record ID
May 22, 2024report date

Recall record at a glance

Official recordZ-1808-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmWishbone Medical, Inc.
Report dateMay 22, 2024
Recall initiation dateApr 5, 2024
Quantity60 units
LocationWarsaw, IN, United States

Official product description

WishFIX Growth Control Plating System, Model Number: TEFCS28-080US. Orthopedic device.

Why the product 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.

Distribution information

US distribution to Florida, New Jersey and Connecticut.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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