Recall On Hernia Mesh Patch | Kugel Mesh Lawyer
In December 2005 the manufacturer of the Kugel mesh patch and the FDA announced a recall of certain lot numbers of the Kugel patch. The recall was later expanded to include additional products and lot numbers. The Bard announcement is reprinted below.
Bard Announces Recall of Composix® Kugel® Mesh X-Large Patch
MURRAY HILL, NJ — (January 13, 2006) — C. R. Bard, Inc. (NYSE-BCR) today announced that it is voluntarily recalling its Bard Composix Kugel Mesh X-Large Patch intended for ventral hernia repair. This recall does not affect any of the company’s other hernia repair products.
The company is initiating this recall due to reports that the device’s plastic coil ring, designed to aid in its deployment, may not withstand the increased stress associated with certain surgical placement techniques. The company has received 24 reports of broken rings out of approximately 32,000 units sold since 2002, a rate of approximately 0.08%.
The products affected by this recall were distributed to customers worldwide. Bard has notified affected customers and the appropriate regulatory agencies, including the U.S. Food and Drug Administration.
The three product codes involved generated sales of approximately $11 million in 2005, before the effect of the recall.
The company expects to record a sales reduction and related charges associated with the recall in the 2005 fourth quarter and these adjustments will cause the company’s results to be below previously stated guidance for the quarter. The company remains comfortable with its previously stated guidance for 2006 of constant currency net sales growth of between 9 percent and 10 percent and diluted earnings per share equivalent to a minimum of $3.42, excluding the effect of FAS123R.
C. R. Bard, Inc. (http://www.crbard.com/), headquartered in Murray Hill, N.J., is a leading multinational developer, manufacturer, and marketer of innovative, life-enhancing medical technologies in the fields of vascular, urology, oncology and surgical specialty products.
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If you or a loved one have been injured by the Kugel Mesh Patch lead please contact us immediately. You may be entitled to compensation.
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The Bard Composix Kugel hernia mesh was removed from the market in December 2005. The Kugel patch recall was later expanded in January 2007 to include additional lot numbers. The hernia mesh recall was due to hernia mesh complications caused by the possibility of the mesh’s “memory recoil ring” breaking. If the ring breaks it [...]
Kugel Mesh Repair
The Kugel hernia mesh patch is used during hernia surgery for several types of repair procedures including:
• Inguinal
• Ventral
• Laparoscopic
The most common type of hernia repair is the ventral where the folded mesh patch is placed behind the hernia through a small incision. After the patch is properly inserted it springs open through [...]
In December 2005 the manufacturer of the Kugel mesh patch and the FDA announced a recall of certain lot numbers of the Kugel patch. The recall was later expanded to include additional products and lot numbers. The Bard announcement is reprinted below.
Bard Announces Recall of Composix® Kugel® Mesh X-Large Patch
MURRAY HILL, NJ — (January 13, [...]
In 2005 Davol, Inc. announced a recall on hernia mesh patch lot numbers 0010206, 0010207, 0010208, 0010209, 0010202 and 0010204 for their Kugel hernia mesh used in hernia repair surgery. This hernia mesh recall was later expanded in January 2007 to include additional product codes and lot numbers.
Here is a timeline of major events in [...]
