TriMed Inc.: Medical Device Recall in 2019 - (Recall #: Z-0118-2020)

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 Dorsal Wrist Hook Plate, Dorsal, 4-Hole, REF WHD-4, contained in a tray, insert, or poly package containing varying amounts, Nonsterile, Single Use Only, Rx. The firm name on the label is TriMed, Santa Clarita, CA.

Product Classification:

Class II

Date Initiated: August 24, 2018

Date Posted: October 16, 2019

Recall Number: Z-0118-2020

Event ID: 83563

Reason for Recall:

Modifications to the specification were not appropriately qualified through the company's design control process which may result in structural integrity issues of the device.

Status: Terminated

Product Quantity: 5 devices

Code Information:

Lot numbers 28884, 28885, 28886, and 28887

Distribution Pattern:

Distribution was made to CA, FL, MD, TX, and WA. There was military and foreign distribution was made to Australia. There was no government distribution.

Voluntary or Mandated:

Voluntary: Firm initiated