Z-1192-2015 Class II Terminated

Recalled by Navilyst Medical, Inc — Glens Falls, NY

Recall Details

Product Type
Devices
Report Date
March 4, 2015
Initiation Date
January 9, 2015
Termination Date
March 10, 2017
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
2 units

Product Description

NAMIC Convenience Kit, LEFT HEART KIT, UPN H965600125911, REF/Catalog No. 60012591, STERILE, Rx ONLY ---For single use only. --- Device Listing Number D136588. NAMIC Convenience Kits are intended to be used in Fluid Management and/or Invasive Pressure Monitoring Systems.

Reason for Recall

The labelled expiration dating of the affected product is not fully supported by shelf life verification testing, which may result in a sterility breach. Use of a Fluid Management Convenience Kit, where sterility has been breached, may result in an increased risk of infection.

Distribution Pattern

Worldwide Distribution - US Nationwide and the countries of: Canada, and Guam.

Code Information

Lot 4440346