C-Qur Mesh made by Atrium is used primarily in hernia repair surgeries to support weakened tissue and to prevent recurring hernias. C-Qur Mesh is also used to support tissue in traumatic wounds, surgical wounds, and chest wall reconstruction. In 2012 The Food and Drug Administration (FDA) issued a warning letter to Atrium regarding improper sterilization and failing to investigate other complaints. In 2013 the FDA issued a recall on all shapes and sizes of C-Qur Mesh, C-Qur Tacshield Mesh, C-Qur V-Patch Mesh and C-Qur Edge Mesh. The most common complications with Atrium’s C-Qur mesh are: additional surgeries to treat hernia recurrence, additional surgeries to treat a mesh related failure or injury, adhesions, bacterial infections, mesh migration, obstructions, pain, and swelling.