PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: May 22, 2024 Initiated: March 19, 2024 #Z-1792-2024

Product Description

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 for Recall

Nail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque.

Details

Recalling Firm
TriMed Inc.
Units Affected
120 units
Distribution
US Nationwide distribution in the states of AK, AR, AZ, CA, FL, HI, IL, LA, MA, MI, NC, NJ, NV, OH, OK, PA, TN, TX, UT, VA, WA, WI.
Location
Santa Clarita, CA

Frequently Asked Questions

What product was 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. Recalled by TriMed Inc.. Units affected: 120 units.
Why was this product recalled?
Nail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque.
Which agency issued this recall?
This recall was issued by the FDA Devices on May 22, 2024. Severity: Moderate. Recall number: Z-1792-2024.