FDAMay 20, 2025device

My3D Personalized Solutions Humeral Cup, Model Number: C24-0223-0003. It is a component of a Custom Constrained Shoulder Arthroplasty Device

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Required inspections were not performed on finished product prior to release and distribution.

What to do

FDA enforcement status: Ongoing

Brands named

onkos surgicalonkos

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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