Atrium Medical Corporation: Medical Device Recall in 2013 - (Recall #: Z-1938-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

C-QUR V-Patch Mesh (All sizes and shapes). Intended for use in soft tissue deficiencies.

Product Classification:

Class II

Date Initiated: July 19, 2013

Date Posted: August 21, 2013

Recall Number: Z-1938-2013

Event ID: 65698

Reason for Recall:

Additional Instructions for Use and Storage Conditions as Coated mesh can adhere to the inner packaging liner due to exposure to high humidity conditions

Status: Terminated

Product Quantity: 95,286 units

Code Information:

Product lines with lot number 10405513 and higher

Distribution Pattern:

USA (nationwide) including Puerto Rico and the countries of Australia Austria Bahrain Brazil Canada Chile Colombia Dominican Republic Ecuador El Salvador France Germany Great Britain Greece Honduras Hong Kong India Ireland Israel Italy Japan Jordan Korea Malaysia Mexico Netherlands New Zealand Nicaragua Norway Panama Peru Portugal Romania Saudi Arabia Singapore South Africa Spain Sri Lanka Switzerland Taiwan Thailand Turkey and Venezuela.

Voluntary or Mandated:

Voluntary: Firm initiated