Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Femoral Resurfacing Cup - (xx)MM Recalled by Synovo Production Due to Medical device components were marketed without FDA clearance...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Synovo Production directly.
Affected Products
Femoral Resurfacing Cup - (xx)MM, Ti-6AI-4V ELI, TiN CERAMIC W/ PLASMA SPRAY, STERILEEO, Reference Numbers: 01-03-0042 01-03-0044 01-03-0045 01-03-0047 01-03-0049 01-03-0051 01-03-0052
Quantity: 496 units
Why Was This Recalled?
Medical device components were marketed without FDA clearance
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Synovo Production
Synovo Production has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report