Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
UOC Femoral Driver Recalled by United Orthopedic Corporation Due to The locking lever pin component of the femoral...
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 United Orthopedic Corporation directly.
Affected Products
UOC Femoral Driver, Product number PE 93045101, orthopedic manual surgical instrument/accessory for use during surgery to implant femoral components and femoral trial, and to remove femoral trial.
Quantity: 33 units
Why Was This Recalled?
The locking lever pin component of the femoral driver may become deformed and break, resulting in malfunction during surgery and causing the device to become inoperable.
Where Was This Sold?
This product was distributed to 1 state: CA
About United Orthopedic Corporation
United Orthopedic Corporation has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report