# FDA recall Z-2777-2020

> **Smith & Nephew, Inc.** · Class II · device recall initiated 2020-06-29.

## 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.

## Reason for recall

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

## Distribution

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

## Key facts

- **Recall number:** Z-2777-2020
- **Recalling firm:** Smith & Nephew, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-06-29
- **Report date:** 2020-08-19
- **Termination date:** 2022-02-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Memphis, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2777-2020

## Citation

> AI Analytics. FDA recall Z-2777-2020. Retrieved 2026-07-17 from https://api.ai-analytics.org/recall/Z-2777-2020. Source: US FDA. Licensed CC0.

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