Reported Mar 4, 2015 · Terminated

NAMIC Convenience Kit, DYE CATH LAB KIT, UPN H749601367131, REF/Catalog No. 60136713, STERILE, Rx ONLY --- For single…

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, DYE CATH LAB KIT, UPN H749601367131, REF/Catalog No. 60136713, 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 4245041
    • 4252386
    • 4264488
    • 4268495
    • 4309476
    • 4345299
    • 4348476
    • 4380280
    • 4394034
    • 4419651
    • 4436717
    • 4447629
    • 4462923
    • 4475805
    • 4505511
    • 4535484
    • 4562284
    • 4573288
    • 4603997
    • 4612732
    • 4614157
    • 4623931
    • 4640168
    • 4648179
    • 4649858
    • 4655616
    • 4661388
    • 4662524
    • 4665312
    • 4675131
    • 4676801
    • 4680698
    • 4681640
    • 4690188
    • 4697403
    • 4704635
    • 4709841
    • 4719502
    • 4728772
    • 4730802
    • 4732490
    • 4742134
    • 4751285
    • 4751286
    • 4764246
    • 4771396
    • 4786638
    • 4790837
    • 4798283
    • 4807655
    • 4817054
    • 4825292
Amount recalled
512 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, 5:31 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.