Z-1202-2015 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
74 units

Product Description

NAMIC Convenience Kit, UPN H965601931651, REF/Catalog No. 60193165, 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

Lots 4639731, 4645195, 4657980, 4661601, 4664394, 4677511, 4786821, 4820468, 4821432, 4832181.