Class II — Potential Health Hazard

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

Composix L/P with Echo PS 10" X 13" Product Code Recalled by Davol, Inc., Subs. C. R. Bard, Inc. Due to Product labeling does not match product configuration.

Date: January 3, 2014
Company: Davol, Inc., Subs. C. R. Bard, 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 Davol, Inc., Subs. C. R. Bard, Inc. directly.

Affected Products

Composix L/P with Echo PS 10" X 13" Product Code 0144113 The Composix L/P Mesh with Echo PS Positioning System is a non-absorbable sterile lightweight mesh prosthesis, with a preattached removable positioning system. This system is indicated and designed for the reconstruction of soft tissue deficiencies during laproscopic ventral hernia repair.

Quantity: 19

Why Was This Recalled?

Product labeling does not match product configuration.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Davol, Inc., Subs. C. R. Bard, Inc.

Davol, Inc., Subs. C. R. Bard, Inc. has 20 total recalls tracked by RecallDetector.

Related Recalls

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