Smith & Nephew, Inc.: Medical Device Recall in 2020 - (Recall #: Z-2777-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

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.

Product Classification:

Class II

Date Initiated: June 29, 2020

Date Posted: August 19, 2020

Recall Number: Z-2777-2020

Event ID: 85946

Reason for Recall:

The 4.5MM PeriLoc Targeter right hand part was anodized green and was marked as a left-hand part.

Status: Terminated

Product Quantity: 3 units

Code Information:

Product Number: 71173400, Lot Number: 16GM20026

Distribution Pattern:

U.S Nationwide including in the states of IN and TN.

Voluntary or Mandated:

Voluntary: Firm initiated