Z-1158-2015 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
454 units

Product Description

NAMIC Convenience Kit, LEFT HEART KIT, UPN H7496005001131, REF/Catalog No. 600500113, STERILE, Rx ONLY --- For single use only. --- Device Listing Number D136588. Product Usage: 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 4247589, 4269253, 4271313, 4310122, 4342473, 4344822, 4387486, 4388838, 4414801, 4419289, 4437439, 4447579, 4474969, 4491873, 4504923, 4534887, 4534888, 4572805, 4604160, 4612239, 4624081, 4640706, 4641690, 4649150, 4651400, 4655126, 4660971, 4662034, 4666092, 4672688, 4680286, 4682905, 4690303, 4697126, 4697804, 4705250, 4708240, 4712693, 4721403, 4731034, 4742373, 4799479, 4807935, 4810688, 4814038, 4814614.