FDA Device recall Z-1791-2024
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-…
- FDA Device
- Class II
- ongoing
- Published 2024-05-22
On 2024-05-22 the FDA classified a Class II recall of 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-… by Trimed, citing nail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1791-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-03-19 |
| Published | 2024-05-22 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Trimed |
| Distribution | US |
Product
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
Reason
Nail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque.
Identifiers
| code_info | UDI: 00842188127878/ Lot # QM23086 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1791-2024%22
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