RecallRadar

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-…

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

AgencyFDA Device
Recall numberZ-1791-2024
ClassificationClass II
Statusongoing
Initiated2024-03-19
Published2024-05-22
Last updated2026-09-13 11:57 UTC
CompanyTrimed
DistributionUS

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_infoUDI: 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

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.