Reported Oct 26, 2016 · Terminated

Arthroscopy Pack, Kit numbers AMS2938, AMS3639, PSS1592(B, PSS1799, and PSS1845(A. convenience custom kits used for…

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?

  • Arthroscopy Pack, Kit numbers AMS2938, AMS3639, PSS1592(B, PSS1799, and PSS1845(A. convenience custom kits used for general surgery in hospital operating room
Lot codes and dates
  • Lot Numbers/ Expiration Dates

    222 of 222 codes

    • 66444
    • 2/5/2015
    • 73046
    • 1/1/2016
    • 74702
    • 3/18/2016
    • 73595
    • 4/17/2016
    • 78038
    • 7/30/2016
    • 76691
    • 9/1/2016
    • 78555
    • 9/11/2016
    • 78554
    • 10/19/2016
    • 56085
    • 6/6/2016
    • 59697
    • 8/1/2015
    • 67248
    • 7/16/2016
    • 68753
    • 9/12/2016
    • 69101
    • 9/3/2016
    • 78129
    • 8/23/2017
    • 80761
    • 2/1/2018
    • 60666
    • 10/19/2014
    • 59667
    • 7/19/2015
    • 60265
    • 7/19/2015
    • 60266
    • 7/22/2015
    • 60267
    • 7/24/2015
    • 61386
    • 8/20/2015
    • 60268
    • 8/25/2015
    • 60269
    • 8/26/2015
    • 61384
    • 9/17/2015
    • 61385
    • 9/27/2015
    • 61388
    • 10/13/2015
    • 61389
    • 10/15/2015
    • 65208
    • 10/19/2015
    • 61387
    • 11/7/2015
    • 63013
    • 11/14/2015
Amount recalled
5723 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, 4:49 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.