Reported Mar 8, 2017 · Terminated

General Pack, part number AMS2967(A General Pack, part number AMS3239(A General Pack, part number AMS3709(B General…

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?

    • General Pack
    • part number AMS2967(A General Pack
    • part number AMS3239(A General Pack
    • part number AMS3709(B General Pack
    • part number AMS5341 General Pack
    • part number AMS5694
Lot codes and dates
    • Lot number and expiration date 100415
    • 9/23/2019 100737
    • 9/30/2019 100981
    • 10/20/2019 101069
    • 9/6/2019 101739
    • 10/19/2019 101816
    • 10/14/2019 83797
    • 5/12/2018 84203
    • 5/26/2018 84668
    • 5/17/2018 84793
    • 2/3/2019 85141
    • 6/8/2018 85421
    • 7/28/2018 85504
    • 8/30/2018 86008
    • 7/8/2018 86260
    • 9/9/2018 86481
    • 9/5/2018 86586
    • 9/27/2018 86774
    • 8/8/2018 86837
    • 9/12/2018 87291
    • 9/30/2018 87456
    • 9/30/2018 87754
    • 1/7/2019 88321
    • 9/6/2018 88648
    • 12/29/2018 88657
    • 12/2/2018 88764
    • 10/8/2018 89333
    • 12/25/2018 89429
    • 12/29/2018 94713
    • 12/14/2018 94739
    • 1/25/2019 94783
    • 12/16/2018 95286
    • 11/12/2018 95349
    • 1/10/2019 95432
    • 1/24/2019 95459
    • 1/21/2019 95928
    • 1/23/2019 95999
    • 3/9/2019 96009
    • 1/7/2019 96501
    • 1/6/2019 96934
    • 5/30/2019 97201
    • 5/5/2019 97338
    • 5/13/2019 97459
    • 6/4/2019 97854
    • 6/14/2019 98176
    • 6/29/2019 98263
    • 6/11/2019 98677
    • 6/3/2019 99291
    • 6/12/2019 99385
    • 6/11/2019 99682
    • 6/29/2019 99712
    • 6/5/2019 99889
    • 9/4/2019 99926
    • 9/27/2019
Amount recalled
1501 kits

This recall covers 124 products

The agency filed one notice per product. You are reading one of them; the other 123 are below.

111 more are in the archive.

Where it was sold

Why it was recalled

The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits 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 May 3, 2017 · Data as of Sep 19, 5:22 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.