FDAFDA · Food and drugs·Recall number Z-2777-2020
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.
Published August 19, 2020 · Recall initiated: June 29, 2020
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The 4.5MM PeriLoc Targeter right hand part was anodized green and was marked as a left-hand part.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Smith & Nephew, Inc.
- Distributor
- U.S Nationwide including in the states of IN and TN.
- Lot
- Product Number: 71173400, Lot Number: 16GM20026
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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