Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

TriMed Peg Guide Extender Recalled by TriMed Inc. Due to The spring on the PEG-Extender can rust due...

Date: September 28, 2018
Company: TriMed Inc.
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact TriMed Inc. directly.

Affected Products

TriMed Peg Guide Extender, REF PEG-XTNDR, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.

Quantity: 1,903 Peg Guide Extenders

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About TriMed Inc.

TriMed Inc. has 18 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report