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Recall Observatory FDA recall evidence

Device product

NAMIC Convenience Kit, MOBILE CATH LAB KIT, UPN H749600419211, REF/Catalog No. 60041921, 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.

Z-1157-2015

January 09, 2015

Class II

Product summary

Firm
Navilyst Medical, Inc
Event
Event 70322
Status
Terminated
Classification
Class II
Quantity
16 units
Official record key
device-enforcement:Z-1157-2015

Official wording

Reason: 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.

Code information: Lots 4346227, 4510688, 4644193, 4692124, 4694166.

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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.