Wishbone Medical, Inc. FDA Recalls

3 recalls on file across devices, 0 of them Class I and 2 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
WishFIX Growth Control Plating System, Model Number: TEFCS28-080US. Orthopedic device.Class IIApr 5, 2024The products in this lot are incorrectly packed with a Stain	The products in this lot are incorrectly packed with a Stainless-Steel implant instead of a Titanium implant a	Class IIDevices	Apr 5, 2024
WishBone Medical Smart Correction Dual Joint Express Struts, external skeleton fixation device Type Part NumbClass IIJan 4, 2023Firm identified that user may be unable to adjust the length	Firm identified that user may be unable to adjust the length of the Smart Correction Dual Joint Express Struts	Class IIDevices	Jan 4, 2023
WishBone Medical Plate and Screw System - Screw, Fixation, Bone, Washer, Bolt Nut. Part Number: PK-SMC0635NL-TI-US, PKClass IIApr 30, 2021Nonconformities were discovered to the engineering specifica	Nonconformities were discovered to the engineering specifications for implant plates and screws.	Class IIDevices	Apr 30, 2021