TriMed Inc.: Medical Device Recall in 2019 - (Recall #: Z-0357-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

TriMed Hex Driver 1.2, 55mm AO Cannulated, REF HXDRIVR-1.2C AO, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.

Product Classification:

Class II

Date Initiated: September 28, 2018

Date Posted: November 20, 2019

Recall Number: Z-0357-2020

Event ID: 83820

Reason for Recall:

The epoxy on Apex manufactured epoxy-coated instruments can pop off.

Status: Ongoing

Product Quantity: 467 hex drivers

Code Information:

Lot numbers 91500604 and 91600017

Distribution Pattern:

Distribution was nationwide. There was military distribution but no government distribution. Foreign distribution was made to Australia, China, South Africa, and Sweden.

Voluntary or Mandated:

Voluntary: Firm initiated