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Smith & Nephew, Inc. recalls PERI-LOC TARGETER 4.5MM DISTAL FEMUR, HANDLE, LEFT, NON-STERILE - Product Usage: used for adult and pediatric patients,
Recalled August 19, 2020 · FDA recall Z-2777-2020 · Smith & Nephew
Hazard
The 4.5MM PeriLoc Targeter right hand part was anodized green and was marked as a left-hand part. · FDA Class II
Units
3 units
Sold at
U.S Nationwide including in the states of IN and TN.
Description
The 4.5MM PeriLoc Targeter right hand part was anodized green and was marked as a left-hand part.
Product
PERI-LOC TARGETER 4.5MM DISTAL FEMUR, HANDLE, LEFT, NON-STERILE - Product Usage: used for adult and pediatric patients, as well as patients with osteopenic bone. PERI-LOC plates and screws are indicated for fixation of pelvic, small and long bone fractures, including those of the tibia, fibula, femur, pelvis, acetabulum, metacarpals, metatarsals, humerus, ulna, radius, calcaneus and clavicle.
Manufacturer(s)
Smith & Nephew, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →