PERI-LOC TARGETER 4 — Class II medical device recall Z-2777-2020
Terminated recall by Smith & Nephew, Inc., reported 2020-08-19, distributed nationwide. The 4.5MM PeriLoc Targeter right hand part was anodized green and was marked as a left-hand part.
| Recall number | Z-2777-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Smith & Nephew, Inc., Memphis, TN, United States |
| Recall initiated | 2020-06-29 |
| Classified | 2020-08-10 |
| Reported by FDA | 2020-08-19 |
| Terminated | 2022-02-18 |
| Distributed | Nationwide (US) |
| Quantity | 3 units |
| Lot numbers | 16GM20026 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2777-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.