Drug recall
TriMed, Threaded IM Nail 3.6mm, 60mm, TI, Ref: IMN3.6-60 T, Non Sterile, MD, Rx Only TriMed, Threaded IM Nail…
FDA recall event 94381 · Class II · TriMed Inc.
Key facts
| Event ID | 94381 |
|---|---|
| Recall numbers | Z-1791-2024, Z-1792-2024 |
| Recalling firm | TriMed Inc. |
| Product type | Devices |
| Products | TriMed, Threaded IM Nail 3.6mm, 60mm, TI, Ref: IMN3.6-60 T, Non Sterile, MD, Rx Only TriMed, Threaded IM Nail 3.6mm, 65mm, TI, Ref: IMN3.6-65 T, Non Sterile, MD, Rx Only |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Nail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque. |
| Initiation date | Mar 19, 2024 |
| Report date | May 22, 2024 |
| City | Santa Clarita |
| State | CA |
| Country | United States |
| FEI number | 3001236812 |
At a glance
- 1–9 Products in this recall
- 10–99 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: