TriMed Inc.: Medical Device Recall in 2018 - (Recall #: Z-2877-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Ulnar Osteotomy Compression Plate, Short Model: UOCP-S Product Usage: The UOCP-S is provided non-sterile with the required fixation screws and surgical instrumentation. The TriMed Ulnar Osteotomy Plate is intended for use in osteotomy procedures of the ulna.

Product Classification:

Class II

Date Initiated: April 16, 2018

Date Posted: August 29, 2018

Recall Number: Z-2877-2018

Event ID: 80487

Reason for Recall:

Two instrument holes located on the side of the plate, which act to align the saw guide are located on the wrong side of the plate

Status: Terminated

Product Quantity: 722

Code Information:

Lot Numbers: 10003, 10017

Distribution Pattern:

Worldwide Distribution in the state of TX and countries of Australia, China Sweden

Voluntary or Mandated:

Voluntary: Firm initiated