Class II — Potential Health Hazard

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

Endotrac EPF/EGR Hook/Triangle Blade Kit Recalled by Stryker GmbH Due to The seal integrity of the sterile bag containing...

Date: April 30, 2019
Company: Stryker GmbH
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 Stryker GmbH directly.

Affected Products

Endotrac EPF/EGR Hook/Triangle Blade Kit, Catalogue Number 3056-1

Quantity: 1600

Why Was This Recalled?

The seal integrity of the sterile bag containing the kits may be compromised.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Stryker GmbH

Stryker GmbH has 68 total recalls tracked by RecallDetector.

Related Recalls

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