Hernia mesh is a medical device that is brought to the market to help the patients who are
suffering from a hernia. It is implanted
in the body of the patients to support the wall and lower the possibility of
any further damage.
Though the device brought satisfaction in the lives of some
patients and help them to continue their regular activities, you will find an
opposite picture too. People are suffering from several ill-effects including:
- Pain
- Infection
- Hernia recurrence
- Bowel obstruction
- Adhesion
- Organ perforation
- And many more
Keeping in mind the complications that the product brought in
the lives of the patients, the mesh manufacturers recalled their products in
some of the cases.
Since 2005, more than 200,000 units of hernia mesh are
recalled by the manufacturers. Ethicon ordered a “market withdrawal” taking
mesh off the market without any recall.
Here is a list of hernia mesh recall:
- 2013
145,000 C-QUR units are recalled by Atrium
Medical
- 2007
16,000 Composix Kugel mesh units are recalled
by Bard Davol
- 2005
18,000 Proceed mesh units are recalled by
Ethicon
- 2005 (Expanded in 2006)
31,000 Composix Kugel mesh units are recalled by Bard Davol
Withdrawal
- In 2016, Ethicon removes all Physiomesh Composite Mesh from the market
Would you like to learn more about the recalled mesh? Would you like to file a lawsuit against the manufacturing company for not making people aware of the ill-effects? File a lawsuit with the lawyers of Mesh Hernia Lawsuit. Their lawyers will help you all through the procedure. For further queries, call at 855-817-3922 or visit at http://meshhernia.com/.
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