About The Hernia Patch Recall:
The US Food and Drug Administration along with Davol, Inc., a subsidiary of C.R. Bard, Inc., have recalled Bard Composix Kugel Mesh Patches indicated for the repair of ventral hernias caused by thinning or stretching of scar tissue that forms after hernia surgery.
The patch is placed behind the hernia through a small incision. The patch is then held open by a memory recoil ring that allows the patch to be folded for insertion and to later spring open and lay flat once it is in place.
The ventral hernia repair device was recalled because the memory recoil ring can break, leading to bowel perforation and/or chronic enteric fistulae. The plastic coil ring is designed to aid in its deployment but can break when increased stress is placed on it from certain surgical placement techniques.
According to the FDA Recall Notice "Patients who have been implanted with a Composix Kugel Mesh Patch during hernia surgery should seek medical attention immediately if they experience symptoms that could be associated with ring breakage. These symptoms include: unexplained or persistent abdominal pain, fever, tenderness at the surgery site or other unusual symptoms."
In a March-24-06 recall notice, Bard recommends that health care professionals "immediately discontinue use of the specific product codes and lot numbers listed below. Additionally, please immediately distribute copies of this Important Patient Management Information to clinicians who may have implanted, or who may be managing patients already implanted with one of these products under voluntary recall."
The product codes for the Dec-05, Jan-06 and Mar-06 recalls are:
| PC#0010206 |
Bard Composix Kugel |
Extra Large Oval |
8.7" x 10.7" |
| PC#0010207 |
Bard Composix Kugel |
Extra Large Oval |
10.8" x 13.7" |
| PC#0010208 |
Bard Composix Kugel |
Extra Large Oval |
7.7" x 9.7" |
| PC#0010209 |
Bard Composix Kugel |
Oval |
6.3" x 12.3" |
| PC#0010202 |
Bard Composix Kugel Large |
Oval |
5.4" x 7" |
| PC#0010204 |
Bard Composix Kugel |
Large Circle |
4.5" |
Class 1 Recall: Bard Composix Kugel Mesh Patch - Expansion
Date Recall
Initiated: |
December 22, 2005 |
Product: |
*This recall notice was updated on January 24, 2007, to include additional product codes and lot numbers recalled by the manufacturer since the first list was issued. The expanded list below includes all recalled product codes and lot numbers.*
| Product Code |
Description |
Lot Numbers Recalled |
Date Recalled |
| 0010206 |
Bard® Composix® Kugel® Extra Large Oval, 8.7” x 10.7” |
All Lot Numbers manufactured before January 2006 |
December 2005 and January 2006 |
| 0010207 |
Bard® Composix® Kugel® Extra Large Oval, 10.8” x 13.7”
|
All Lot Numbers manufactured before January 2006 |
December 2005 and January 2006 |
| 0010208 |
Bard® Composix® Kugel® Extra Large Oval, 7.7” x 9.7” |
All Lot Numbers manufactured before January 2006 |
December 2005 and January 2006 |
| 0010209 |
Bard® Composix® Kugel® Oval, 6.3” x 12.3” |
All Lot Numbers manufactured before March 2006 |
March, 24, 2006 |
| 0010202 |
Bard® Composix® Kugel® Large Oval, 5.4” x 7.0” |
Lot Numbers manufactured before October 2005 (see below) |
January 10, 2007 |
| 0010204 |
Bard® Composix® Kugel® Large Circle, 4.5” |
Lot Numbers manufactured before October 2005 (see below) |
January 10, 2007 |
|
Recalling Firm: |
Davol, Inc., Sub. C.R. Bard, Inc.
100 Sockanossett Crossroad
Cranston, RI 02920 |
Reason for Recall: |
The "memory recoil ring" that opens the Bard® Composix® Kugel® Mesh Patch can break under the stress of placement of the large sized products in the intra-abdominal (inside the belly area) space. This can lead to bowel perforations (rupture) and/or chronic (recurring) intestinal fistulae (abnormal connections or passageways between the intestines and other organs). |
Public Contact: |
Robin Drago
VP Regulatory & Clinical Affairs
Davol, Inc., Sub. C.R. Bard, Inc.
100 Sockanossett Crossroad
Cranston, RI 02920
401-463-7000 |
FDA District: |
New England |
FDA Comments: |
- On January 10, 2007, Davol, Inc. (a subsidiary of C.R. Bard) sent letters to health care professionals and distributors notifying them of the most recent expansion of this recall of specific lots of Bard ® Composix ® Kugel ® Large Oval and Large CircleMesh Patches for product codes 0010202 and 0010204. Surgeons and hospitals should stop using the recalled product and return unused units to the company.
- Patients who have been implanted with one of the recalled devices should seek medical attention immediately if they experience symptoms that could be associated with ring breakage such as unexplained or persistent abdominal pain, fever, tenderness at the implant site or other unusual symptoms.
- It should be noted that product codes 0010202 and 0010204 were involved in both recall expansions. The lots manufactured prior to January 2004 were recalled during the March 2006 expansion. Since the March expansion, Davol received 4 confirmed complaints of recoil ring breakage from product code 0010202 manufactured between January 2004 and September 2005. There were no complaints for product code 0010204 . Davol is recalling the following lotsfor product codes0010202 and 0010204:
- All lots with the letter “O” in the fourth position
- All lots with the letter “P” in the fourth position and the letters “A” through “I” in the third position.
For instance, an example of a recalled lot number is “43IPD###.”
- Davol also decided to withdraw from the market specific lots of 0010202 and 0010204 manufactured from October 2005 to October 2006. A market withdrawal is a firm’s removal or correction of a distributed product that involves a minor violation or no violation of the law and would not be subject to legal action by the FDA. Davol is withdrawing the following lots:
- All lots with the letter “P” in the fourth position and the letters “J” through “L” in the third position
- All lots with the letter “Q” in the fourth position and the letters “A” through “I” in the third position
For instance, an example of a withdrawn lot number is “43IQD###.”
- An upgraded product design for both product codes is available for replacement. Product codes and lot numbers that contain the re-designed product can easily be identified on the case or unit package with the label stating “Redesigned for improved ring integrity.” If this label is affixed to your case stock and/or individual packages, this product is not affected by this market withdrawal and need not be returned to Davol.
- Davol notified U.S. customers of the initial recall by letter on 12/27/05 via Federal Express. On March 24, 2006, Bard issued letters to hospitals and health care professionals alerting them to the additional recalled products. The letters included updated Instructions for Use (“IFU”) clarifying the proper insertion technique and Supplemental Patient Management Information. Copies of current product IFUs to be used for both Open Placement and Laparoscopic Placement for the Large Bard ®Composix ® Kugel ® Mesh Patches are available from Davol Customer Service by calling 1-800-531-4124.
- For more information, customers can contact Davol Customer Service at 1-800-531-4124. Physicians may contact Bard’s Medical Services and Support Department at 1-800-562-0027 or to speak with the Bard Medical Director, call 1-908-277-8306.
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Bard Composix Hernia Patch News Archive>>>>
The Scope MDL 07-1842 patch has alleged defects associated with the Bard Composix Kugel Hernia Patches, product codes 0010201-0010209. On February 12th, 2008 the Rhode Island federal District Court ordered that all Davol ring and dual mesh hernia meshes be included with the expanded patch Scope MDL 07-1842 in Rhode Island.
If you or a loved one have
been injured as a result of a defective hernia repair patch or a recalled hernia repair patch you may be entitled to compensation. Contact the bard Composix Kugel Hernia Patch attorneys of Ennis & Ennis today for a free confidential case evaluation. Our on staff nurse and lawyers are standing by to answer any questions you may have regarding the repair patch, a possible Hernia Patch class action lawsuit, or any other type of Bard Composix Kugel Hernia Patch litigation.
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