Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PERI-LOC TARGETER 4.5MM DISTAL FEMUR Recalled by Smith & Nephew, Inc. Due to The 4.5MM PeriLoc Targeter right hand part was...
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 Smith & Nephew, Inc. directly.
Affected Products
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.
Quantity: 3 units
Why Was This Recalled?
The 4.5MM PeriLoc Targeter right hand part was anodized green and was marked as a left-hand part.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Smith & Nephew, Inc.
Smith & Nephew, Inc. has 220 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report