Reported Mar 8, 2017 · Terminated

Arthroscopy Pack, part number AMS2938 Arthroscopy Pack, part number AMS3639 Arthroscopy Pack, part number AMS4765…

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
    • part number AMS2938 Arthroscopy Pack
    • part number AMS3639 Arthroscopy Pack
    • part number AMS4765 Arthroscopy Pack
    • part number PSS1799 Arthroscopy Pack
    • part number PSS1845(A
Lot codes and dates
    • Lot Numbers and Expiration Dates 83622
    • 5/19/2018 84374
    • 5/24/2018 84729
    • 5/17/2017 84897
    • 5/26/2018 84946
    • 6/24/2017 85171
    • 6/9/2018 85363
    • 7/20/2017 85548
    • 7/15/2018 85696
    • 8/22/2018 85698
    • 7/21/2017 86510
    • 9/29/2018 86687
    • 9/5/2018 86889
    • 7/11/2017 86909
    • 9/12/2018 87156
    • 8/1/2018 87157
    • 9/5/2018 87159
    • 10/23/2017 87289
    • 10/17/2017 87978
    • 10/31/2017 88401
    • 10/7/2017 88549
    • 10/28/2017 88656
    • 12/7/2017 89219
    • 12/22/2017 89904
    • 1/23/2017 94742
    • 12/29/2017 95143
    • 12/4/2017 95284
    • 2/2/2018 95315
    • 2/20/2018 95840
    • 2/13/2018 96006
    • 1/7/2018 96469
    • 2/27/2018 96631
    • 1/8/2018 96821
    • 3/25/2018 96931
    • 2/1/2018 97751
    • 3/2/2018 98923
    • 3/20/2018 98971
    • 9/19/2018
Amount recalled
1,081 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, 4:50 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.