Reported Mar 4, 2015 · Terminated

NAMIC Convenience Kit, LEFT HEART KIT, UPN H749600407061, REF/Catalog No. 60040706, STERILE, Rx ONLY --- For single use…

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 KIT, UPN H749600407061, REF/Catalog No. 60040706, 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 4281038
    • 4309507
    • 4316974
    • 4345324
    • 4391599
    • 4394037
    • 4413639
    • 4437396
    • 4445586
    • 4462921
    • 4487772
    • 4491909
    • 4535424
    • 4573282
    • 4604031
    • 4611496
    • 4612705
    • 4621526
    • 4637682
    • 4641685
    • 4642795
    • 4649887
    • 4655637
    • 4662091
    • 4666229
    • 4673307
    • 4673972
    • 4680960
    • 4685521
    • 4689891
    • 4691475
    • 4696324
    • 4696697
    • 4704058
    • 4707554
    • 4709840
    • 4715431
    • 4719309
    • 4723227
    • 4729582
    • 4735756
    • 4743050
    • 4751064
    • 4761328
    • 4764903
    • 4770755
    • 4785895
    • 4811466
    • 4814714
    • 4817065
    • 4821059
    • 4826601
    • 4832365
Amount recalled
489 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, 4:50 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.