Composix Hernia Patch

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Composix Hernia Patch Recall

Between December 2005 and January 2007, four Composix Kugel Mesh Patch recalls were initiated by the product manufacturer—Davol, Inc.—because of device defects . The recalls were prompted by numerous reports of broken recoil rings, which are responsible for opening the patch once it has been surgically implanted in a patient. Unfortunately, this Composix Kugel Mesh Patch defect can cause a patient to suffer abdominal pain, chronic intestinal fistulae (abnormal passages between organs/intestines) and bowel perforations.

If you have been implanted with the Composix Kugel Mesh Patch and suffered an adverse reaction as a consequence, you should consult with an experienced product liability lawyer who can determine your eligibility to recover compensation for your injuries.

Recalled Product Codes & Lot Numbers

Composix Kugel Extra Large Oval (8.7” x 10.7”)—Product Code 0010206, all lot numbers
Composix Kugel Extra Large Oval (10.8” x 13.7”)—Product Code 0010207, all lot numbers
Composix Kugel Extra Large Oval (7.7” x 9.7”)—Product Code 0010208, all lot numbers
Composix Kugel Oval (6.3” x 12.3”)—Product Code 0010209, all lot numbers
Composix Kugel Large Oval (5.4” x 7”)—Product Code 0010202, all lot numbers
Composix Kugel Large Circle (4.5”)—Product Code 0010204, all lot numbers

Injured by a Defective Patch?

If you were implanted with a Composix Kugel Mesh Patch to repair a ventral, or incisional, hernia and have experienced serious side effects such as fever, abdominal pain or tenderness, your device may be defective. Please contact us today for a complimentary consultation with a skilled and understanding personal injury attorney who can evaluate your case and help you plan a course of action.

Product Liability Breaking News

"Hernia Patch Questions"

Late in 2005, C.R.Bard Inc. issued a recall of the composix hernia patch , which is manufactured by its subsidiary, Davol Inc. The recall urged doctors to stop using the larger i...

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