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[Recalled] 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 — Nail system contains an out of specification driver-sock

recall fda device united-states

A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.

Recall details

ProductTriMed, 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
Brand / manufacturerTriMed Inc.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-1791-2024
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date19 March 2024
EAN / barcode00842188127878

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Nail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque.

This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from TriMed Inc.

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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