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 hopital 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.

CLICK HERE FOR THE OFFICIAL PRESS RELEASE FROM C.R. BARD, INC.

CLICK HERE FOR RECALL INFORMATION FROM THE FOOD AND DRUG ADMINISTRATION