Class II — Potential Health Hazard

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

TRYX Neuro Absorbable Antibacterial Envelope Product Usage: Indicated for stabilization Recalled by TYRX Inc. Due to TRYX products are being recalled since the processes...

Date: June 29, 2016
Company: TYRX Inc.
Status: Terminated
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 TYRX Inc. directly.

Affected Products

TRYX Neuro Absorbable Antibacterial Envelope Product Usage: Indicated for stabilization of implanted pacemakers (IPG) and/or implantable cardioverter defibrillators (ICD)

Quantity: 194 units

Why Was This Recalled?

TRYX products are being recalled since the processes of spaying, welding, drying oven and polymer were not adequately validated.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About TYRX Inc.

TYRX Inc. has 3 total recalls tracked by RecallDetector.

Related Recalls

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