Reported Mar 4, 2015 · Terminated

NAMIC Convenience Kit, LEFT HEART CATH KIT, UPN H7496010018151, REF/Catalog No. 601001815, STERILE, Rx ONLY --- For…

Navilyst Medical, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Navilyst Medical, Inc · 10 Glens Falls Technical Park · Glens Falls, NY · 12801

Is this the product you have?

  • NAMIC Convenience Kit, LEFT HEART CATH KIT, UPN H7496010018151, REF/Catalog No. 601001815, STERILE, Rx ONLY --- For single use only. --- Device Listing Number D136588
  • Product UsageNAMIC Convenience Kits are intended to be used in Fluid Management and/or Invasive Pressure Monitoring Systems
Lot codes and dates
    • Lots 4361877
    • 4362670
    • 4384555
    • 4475742
    • 4534905
    • 4534906
    • 4572742
    • 4573424
    • 4603617
    • 4613738
    • 4623233
    • 4641655
    • 4642470
    • 4649930
    • 4654858
    • 4662098
    • 4666862
    • 4667793
    • 4672390
    • 4680972
    • 4681793
    • 4690126
    • 4696307
    • 4702956
    • 4706317
    • 4716358
    • 4726251
    • 4736913
    • 4747725
    • 4766391
    • 4778794
    • 4816062
    • 4820335
    • 4824146
    • 4834213
Amount recalled
62 units

This recall covers 60 products

The agency filed one notice per product. You are reading one of them; the other 59 are below.

47 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Mar 10, 2017 · Data as of Sep 19, 5:33 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.