Drug recall
PERI-LOC TARGETER 4.5MM DISTAL FEMUR, HANDLE, LEFT, NON-STERILE - Product Usage: used for adult and pediatric…
FDA recall event 85946 · Class II · Smith & Nephew, Inc.
Key facts
| Event ID | 85946 |
|---|---|
| Recall numbers | Z-2777-2020 |
| Recalling firm | Smith & Nephew, Inc. |
| Product type | Devices |
| Products | 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The 4.5MM PeriLoc Targeter right hand part was anodized green and was marked as a left-hand part. |
| Initiation date | Jun 29, 2020 |
| Report date | Aug 19, 2020 |
| Termination date | Feb 18, 2022 |
| City | Memphis |
| State | TN |
| Country | United States |
| FEI number | 1020279 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: