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On June 13, 2016, Health Canada issued a recall of Ethicon's Physiomesh Flexible Composite Mesh Product used for ventral hernia repair. [13] The product had been on the Canadian market since September 2010 and patients claimed a range of complications following surgery. [14]
Repairs that utilize mesh are usually the first recommendation for the vast majority of patients including those that undergo laparoscopic repair. [12] Procedures that employ mesh are the most commonly performed as they have been able to demonstrate better results compared to non-mesh repairs. [ 21 ]
Superior Court of California, the Pennsylvania Superior Court has declined to toss a more than $12.8 million judgment against pelvic mesh maker Ethicon. $12.8M Pelvic Mesh Verdict Stands as Pa ...
Prolene is a brand of synthetic polypropylene used in monofilament nonabsorbable sutures and meshes. The suture is indicated for skin closure and general soft tissue approximation and ligation. Its advantages include minimal tissue reactivity and durability.
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The recall involves updating instructions for use rather than removing the device, POLARx Cryoablation Balloon Catheters, from where they are used or sold, the FDA said. The FDA said the use of ...
The devices are used in patients undergoing cardiac and non-cardiac surgery, and to treat those who have had heart failure or have acute coronary syndrome, a group of diseases in which blood flow ...
When herniotomy is combined with a reinforced repair of the posterior inguinal canal wall with autogenous (patient's own tissue) or heterogeneous material such as prolene mesh, it is termed hernioplasty as opposed to herniorrhaphy, in which no autogenous or heterogeneous material is used for reinforcement. [citation needed]