The Phsyiomesh Was Recalled Due To High Failure Rates
Recalled Ethicon Physiomesh Recalled Lots
The action affects the Ethicon Physiomesh Composite Mesh product line. The product codes affected include PHY0715R, PHY1015V, PHY1515Q, PHY1520R, PHY1520V, PHY2025V, PHY2030R, PHY2535V, PHY3035R, and PHY3050R.
The recall does not affect the Ethicon Physiomesh Open Flexible Composite Mesh device or other Ethicon mesh products.
Other companies who issued recalls of their hernia mesh products include:
- Atrium Medical Corporation
- C-Qur Surgical Mesh
- Bard Davol
- Kugel Hernia Patch
Ethicon recalled Proceed on January 4, 2006, January 14, 2011, and April 3, 2014. According to the recall announcement, incomplete seals on the product could lead to delamination and compromised sterility.