Class II — Potential Health Hazard

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

Bard¿ PerFix Light Plug The Bard¿ PerFix Light Plug is Recalled by Davol, Inc., Subs. C. R. Bard, Inc. Due to The patient record peel-off label product code and...

Date: October 8, 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

Bard¿ PerFix Light Plug The Bard¿ PerFix Light Plug is indicated for reinforcement if soft tissue, where weakness exists, in procedures involving soft tissue repair, such as groin hernia defects.

Quantity: 78 units

Why Was This Recalled?

The patient record peel-off label product code and size did not match the other labeling and actual product in the packaging for the Bard Small PerFix Light Plug.

Where Was This Sold?

This product was distributed to 8 states: CA, DE, MD, MN, MO, NM, OH, UT

Affected (8 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