Davol, Inc., Subs. C. R. Bard, Inc.: Medical Device Recall in 2014 - (Recall #: Z-0191-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: October 8, 2014

Date Posted: November 19, 2014

Recall Number: Z-0191-2015

Event ID: 69464

Reason for Recall:

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.

Status: Terminated

Product Quantity: 78 units

Code Information:

Lot# HUYD0176

Distribution Pattern:

US Distribution including the states of CA, NM, OH, DE, MN, UT, MD and MO.

Voluntary or Mandated:

Voluntary: Firm initiated