FDAFDA · Food and drugs·Recall number Z-0191-2015
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.
Published November 19, 2014 · Recall initiated: October 8, 2014
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Davol, Inc., Subs. C. R. Bard, Inc.
- Distributor
- US Distribution including the states of CA, NM, OH, DE, MN, UT, MD and MO.
- Lot
- Lot# HUYD0176
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.