Wishbone Medical, Inc.: Medical Device Recall in 2024 - (Recall #: Z-1808-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: April 5, 2024

Date Posted: May 22, 2024

Recall Number: Z-1808-2024

Event ID: 94405

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.

Status: Ongoing

Product Quantity: 60 units

Code Information:

Model Number: TEFCS28-08-US; UDI/DI: B562TEFCS2808US0; Lot Number: 28042

Distribution Pattern:

US distribution to Florida, New Jersey and Connecticut.

Voluntary or Mandated:

Voluntary: Firm initiated