TriMed Inc.: Medical Device Recall in 2019 - (Recall #: Z-0358-2020)

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 Peg Guide Extender, REF PEG-XTNDR, 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-0358-2020

Event ID: 83820

Reason for Recall:

The spring on the PEG-Extender can rust due to the type of steel used to manufacture it.

Status: Ongoing

Product Quantity: 1,903 Peg Guide Extenders

Code Information:

Lot number 2858, 2861, and 3749

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