TriMed Inc.: Medical Device Recall in 2019 - (Recall #: Z-0359-2020)

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 Wrist Hook Dorsal Impactor, REF IMPCT-WHD; and TriMed Wrist Hook Volar Impactor, REF IMPCT-WHV, both nonsterile, Rx, The firm name on the labels is TriMed Inc., Santa Clarita, CA.

Product Classification:

Class II

Date Initiated: September 28, 2018

Date Posted: November 20, 2019

Recall Number: Z-0359-2020

Event ID: 83820

Reason for Recall:

The WHD/WHV impactors can rust over time due to an improper manufacturing process.

Status: Ongoing

Product Quantity: 561 devices

Code Information:

Lot numbers 049045, 049044, and 049044R1.

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