Reported Oct 26, 2016 · Terminated

Hand Tray PSS2365(A, PSS2365(B, PSS2365(C, PSS2365(D PSS2365(E, convenience custom kits used for general surgery in…

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?

  • Hand Tray PSS2365(A, PSS2365(B, PSS2365(C, PSS2365(D PSS2365(E, convenience custom kits used for general surgery in hospital operating room
Lot codes and dates
  • Lot numbers/Expiration dates

    126 of 126 codes

    • 62742
    • 2/28/2014
    • 65112
    • 3/23/2014
    • 65816
    • 4/24/2014
    • 56706
    • 5/15/2014
    • 66648
    • 7/21/2014
    • 66649
    • 7/21/2014
    • 66165
    • 7/25/2014
    • 57524
    • 9/1/2014
    • 57338
    • 9/20/2014
    • 57977
    • 9/22/2014
    • 56883
    • 9/24/2014
    • 57057
    • 9/24/2014
    • 57523
    • 9/25/2014
    • 58348
    • 1/3/2015
    • 58349
    • 1/4/2015
    • 59680
    • 1/17/2015
    • 60694
    • 1/24/2015
    • 59678
    • 1/25/2015
    • 59679
    • 1/26/2015
    • 59221
    • 1/28/2015
    • 60104
    • 1/29/2015
    • 61738
    • 4/24/2015
    • 61740
    • 6/11/2015
    • 64688
    • 6/19/2015
    • 63590
    • 6/22/2015
    • 63772
    • 6/22/2015
    • 64002
    • 6/22/2015
    • 61739
    • 6/27/2015
    • 63257
    • 6/28/2015
    • 67941
    • 2/11/2016
Amount recalled
3444 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, 4:44 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.