Reported Mar 4, 2015 · Terminated

NAMIC Convenience Kit, UPN H749602301481, REF/Catalog No. 60230148, STERILE, Rx ONLY --- For single use only. ---…

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, UPN H749602301481, REF/Catalog No. 60230148, STERILE, Rx ONLY --- For single use only. --- Device Listing Number D136588. NAMIC Convenience Kits are intended to be used in Fluid Management and/or Invasive Pressure Monitoring Systems.
Lot codes and dates
  • 107 of 107 codes

    • Lots 4245786
    • 4248982
    • 4252309
    • 4260234
    • 4268141
    • 4279218
    • 4288402
    • 4298225
    • 4314481
    • 4320621
    • 4329211
    • 4337129
    • 4344176
    • 4353785
    • 4361710
    • 4372511
    • 4384175
    • 4393701
    • 4398980
    • 4403990
    • 4423304
    • 4457003
    • 4466333
    • 4469607
    • 4476888
    • 4485248
    • 4492442
    • 4498101
    • 4501790
    • 4507503
    • 4514700
    • 4528475
    • 4538380
    • 4548574
    • 4557974
    • 4565199
    • 4575422
    • 4579968
    • 4597587
    • 4613549
    • 4616353
    • 4636559
    • 4639117
    • 4642346
    • 4643978
    • 4644874
    • 4645905
    • 4649110
    • 4651282
    • 4651492
    • 4663423
    • 4667161
    • 4668890
    • 4671604
    • 4675060
    • 4676056
    • 4677276
    • 4678679
    • 4681618
    • 4685667
Amount recalled
2502 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, 6:06 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.