Reported Oct 26, 2016 · Terminated

Basic Tray, Kit part numbers AMS1199(A and PSS1559(A convenience custom kits used for general surgery in hospital…

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?

  • Basic Tray, Kit part numbers AMS1199(A and PSS1559(A convenience custom kits used for general surgery in hospital operating room
Lot codes and dates
  • Lot Numbers/Expiration Dates

    88 of 88 codes

    • 56958
    • 5/29/2016
    • 56991
    • 6/4/2016
    • 57637
    • 7/5/2016
    • 57788
    • 7/10/2016
    • 59063
    • 1/22/2016
    • 59363
    • 3/24/2015
    • 60073
    • 10/30/2016
    • 60752
    • 10/29/2015
    • 61309
    • 9/27/2015
    • 62116
    • 11/28/2015
    • 62453
    • 11/14/2015
    • 62727
    • 11/5/2015
    • 63987
    • 1/8/2016
    • 64556
    • 1/6/2016
    • 65214
    • 1/1/2016
    • 65698
    • 11/30/2015
    • 66531
    • 8/9/2016
    • 66620
    • 11/9/2015
    • 68220
    • 9/28/2016
    • 68650
    • 9/13/2016
    • 69059
    • 9/22/2016
    • 69210
    • 5/26/2016
    • 69417
    • 9/7/2016
    • 69787
    • 1/29/2017
    • 70198
    • 11/30/2016
    • 70590
    • 9/21/2016
    • 70993
    • 12/6/2016
    • 71368
    • 12/13/2016
    • 71904
    • 3/30/2017
    • 72550
    • 1/10/2017
Amount recalled
1599 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, 6:03 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.