Z-2777-2020 Class II Terminated
FDA device recall Z-2777-2020 was initiated by Smith & Nephew, Inc. on June 29, 2020 and is designated Class II. Reason for recall: The 4.5MM PeriLoc Targeter right hand part was anodized green and was marked as a left-hand part. The recall status is terminated (terminated February 18, 2022). Affected quantity: 3 units.
Recall Details
- Product Type
- Devices
- Report Date
- August 19, 2020
- Initiation Date
- June 29, 2020
- Termination Date
- February 18, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 3 units
Product Description
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.
Reason for Recall
The 4.5MM PeriLoc Targeter right hand part was anodized green and was marked as a left-hand part.
Distribution Pattern
U.S Nationwide including in the states of IN and TN.
Code Information
Product Number: 71173400, Lot Number: 16GM20026