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...
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
About Davol, Inc., Subs. C. R. Bard, Inc.
Davol, Inc., Subs. C. R. Bard, Inc. has 20 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report