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United Orthopedic Corporation recalls UOC Femoral Driver, Product number PE 93045101, orthopedic manual surgical instrument/accessory for use during surgery t
Recalled April 5, 2017 · FDA recall Z-1692-2017 · United Orthopedic
Hazard
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. · FDA Class II
Units
33 units
Sold at
Worldwide Distribution - US including State of CA and Internationally to Pakistan, Spain, and Taiwan.
Description
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.
Product
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.
Manufacturer(s)
United Orthopedic Corporation
Made in
Taiwan
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →