Class II — Potential Health Hazard

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

C-QUR Edge Mesh (All sizes and shapes). Intended for use Recalled by Atrium Medical Corporation Due to Additional Instructions for Use and Storage Conditions as...

Date: July 19, 2013
Company: Atrium Medical Corporation
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 Atrium Medical Corporation directly.

Affected Products

C-QUR Edge Mesh (All sizes and shapes). Intended for use in soft tissue deficiencies.

Quantity: 1501 units

Why Was This Recalled?

Additional Instructions for Use and Storage Conditions as Coated mesh can adhere to the inner packaging liner due to exposure to high humidity conditions

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Atrium Medical Corporation

Atrium Medical Corporation has 150 total recalls tracked by RecallDetector.

Related Recalls

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