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BARD COMPOSIX HERNIA PATCH RECALL
The FDA has advised patients who have been implanted with a Bard Composix Kugel Mesh Patch to seek medical attention immediately if they experience unexplained or persistent abdominal pain, fever, tenderness at the implant site or other unusual symptoms. Contact your hernia surgeon and hospital to see if you were implanted with a recalled Bard Composix Kugel Mesh Patch.
THE FOLLOWING BARD COMPOSIX HERNIA PATCHES ARE AFFECTED BY THE FDA RECALL
PRODUCT NO. DESCRIPTION
0010206 Bard Composix Kugel Extra Large Oval 0010207 Bard Composix Kugel Extra Large Oval 0010208 Bard Composix Kugel Extra Large Oval 0010209 Bard Composix Kugel Oval 0010202 Bard Composix Kugel Large Oval 0010204 Bard Composix Kugel Large Circle
If you or someone you know has received one of these recalled hernia patches then you should contact an attorney now to find out if you may be eligible to make a claim for compensation.
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