Reported Oct 26, 2016 · Terminated

Custom Venous Kit, TVS4024(C convenience custom kits used for general surgery in hospital operating room

Windstone Medical Packaging, 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: Windstone Medical Packaging, Inc. · 1602 4th Ave N · Billings, MT · 59101-1521

Is this the product you have?

  • Custom Venous Kit, TVS4024(C convenience custom kits used for general surgery in hospital operating room
Lot codes and dates
  • Lot Numbers Expiration Dates

    62 of 62 codes

    • 57411
    • 5/13/2015
    • 58475
    • 5/14/2015
    • 57820
    • 5/17/2015
    • 60799
    • 8/3/2015
    • 62975
    • 11/14/2015
    • 63103
    • 11/14/2015
    • 62235
    • 11/15/2015
    • 62675
    • 11/25/2015
    • 65935
    • 11/27/2015
    • 60995
    • 11/29/2015
    • 63104
    • 12/14/2015
    • 64487
    • 1/5/2016
    • 63521
    • 1/29/2016
    • 67570
    • 4/30/2016
    • 68694
    • 7/11/2016
    • 69235
    • 7/14/2016
    • 68935
    • 7/18/2016
    • 67788
    • 7/30/2016
    • 70949
    • 9/19/2016
    • 76072
    • 11/2/2016
    • 80515
    • 11/2/2016
    • 74746
    • 11/9/2016
    • 76638
    • 11/25/2016
    • 73892
    • 11/26/2016
    • 75428
    • 11/28/2016
    • 79295
    • 11/30/2016
    • 71620
    • 12/12/2016
    • 70720
    • 1/4/2017
    • 75219
    • 5/31/2017
    • 77663
    • 6/19/2017
Amount recalled
1584 kits

This recall covers 150 products

The agency filed one notice per product. You are reading one of them; the other 149 are below.

137 more are in the archive.

Where it was sold

Why it was recalled

The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the custom AMS kit were recalled because gloves may contain splits or holes compromising sterility.

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Oct 25, 2016 · Data as of Sep 19, 6:02 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.