Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ACETABULAR BEARING (xx)MM I.D X (xx) O.D. UHMWPE 1020 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
ACETABULAR BEARING (xx)MM I.D X (xx) O.D. UHMWPE 1020, STERILEEO, Reference Numbers: 01-02-4254 01-02-4456 01-02-4558 01-02-4760 01-02-4962 01-02-5164 01-02-5266
Quantity: 1681 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