Reported Oct 26, 2016 · Terminated

Knee Arthroscopy Pack AMS2610, AMS2610(A, AMS3236, PSS2188(A, and PSS2208(A convenience custom kits used for 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?

  • Knee Arthroscopy Pack AMS2610, AMS2610(A, AMS3236, PSS2188(A, and PSS2208(A convenience custom kits used for general surgery in hospital operating room
Lot codes and dates
  • Lot Numbers/Expiration Dates
    • 63879
    • 1/23/2014
    • 58286
    • 3/18/2014
    • 58810
    • 6/21/2014
    • 62512
    • 10/18/2014
    • 63024
    • 12/13/2014
    • 65774
    • 2/25/2015
    • 68072
    • 4/17/2015
    • 68548
    • 4/25/2015
    • 70982
    • 11/26/2015
    • 73402
    • 3/14/2016
    • 74837
    • 3/22/2016
    • 75198
    • 4/20/2016
    • 67703
    • 7/1/2016
    • 78551
    • 7/30/2016
    • 78600
    • 7/30/2016
    • 68823
    • 9/11/2016
    • 68713
    • 9/20/2016
    • 71080
    • 12/26/2016
    • 72020
    • 1/10/2017
    • 73647
    • 1/28/2017
    • 73205
    • 3/9/2017
    • 73034
    • 3/23/2017
    • 77621
    • 7/21/2017
    • 79992
    • 8/1/2017
    • 77815
    • 8/11/2017
    • 80859
    • 8/31/2017
    • 77783
    • 10/10/2017
    • 75744
    • 10/21/2017
    • 79326
    • 1/13/2018
Amount recalled
N/A

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.

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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, 5:35 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.