Bard Mesh Recall Lot Numbers

Bard Mesh Recall Lot Numbers – The fda has recalled the composix kugel mesh patch, used to repair ventral. The recall was initiated by davol, inc., sub. Food and drug administration (fda) regulates medical devices and has taken various actions regarding the bard 3dmax hernia mesh. The product was incorrectly labeled as left large.

Include additional product codes and lot numbers in january 2007. Physiomesh isn't the only hernia mesh product with a number of adverse event reports. Defective hernia mesh products that are the subjects of lawsuits can be identified by their product number. 1 02/22/2006 davol, inc., sub.

Bard Mesh Recall Lot Numbers

Bard/davol recalled 232 units of bard 3d max mesh, a polypropylene mesh for hernia repair, due to mislabeling. Some were recalled by the food and drug administration (fda),. From 2005 to february 2019, hernia mesh manufacturers recalled more than 211,000 units of hernia mesh.

The bard composix kugel mesh patch. If you have received a hernia mesh implant and suffered chronic pain or other medical complications, you can turn to your medical records to find which type and model of mesh you received. Terminated 3 on june 06, 2016:

Product code description lot numbers recalled date recalled 0010206 bard® composix® kugel®. Bard has expanded its recall of mesh patches used to repair hernias to include additional lot numbers. The table below provides the hernia mesh recall list updated for 2020:

February 1, 2007 1 min read c.r. Explore more than 120,000 recalls, safety alerts and field safety notices of medical devices and their connections with their manufacturers. This is an active lawsuit see if you qualify the fda.

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