Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Versafitcup Impacting Ring Model Number: 01.26.10.0133 (46mm) Recalled by Medacta Usa Inc Due to Medacta USA is recalling Versafitcup Impacting Ring because...
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 Medacta Usa Inc directly.
Affected Products
Versafitcup Impacting Ring Model Number: 01.26.10.0133 (46mm), 01.26.10.0134 (48mm), 01.26.10.0135 (50mm), 01.26.10.0136 (52mm), 01.26.10.0137 (54mm), 01.26.10.0138 (56mm), 01.26.10.0139 (58mm), 01.26.10.0140 (60mm), 01.26.10.0141 (62mm), 01.26.10.0142 (64mm). Designed for cementless use in total hip arthroplasty.
Quantity: 293 units
Why Was This Recalled?
Medacta USA is recalling Versafitcup Impacting Ring because the impaction ring may not fit properly in the implant shell in all cases. This could result in surgical delay potentially increasing possible complications under anesthesia, having to ream up to a larger shell size leaving less bone than planned and repositiong/removal of the shell after initial impaction.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medacta Usa Inc
Medacta Usa Inc has 16 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report