Reported Mar 8, 2017 · Terminated

Spine Pack , part number AMS3753(A Spine Pack, part number AMS3783(A Spine Pack, part number AMS3783(B Spine Pack, part…

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?

    • Spine Pack
    • part number AMS3753(A Spine Pack
    • part number AMS3783(A Spine Pack
    • part number AMS3783(B Spine Pack
    • part number AMS6472
Lot codes and dates
    • Lot number and expiration date 100932
    • 1/28/2018 101802
    • 11/13/2018 84360
    • 6/3/2017 85663
    • 7/20/2017 86544
    • 7/4/2017 87130
    • 8/24/2017 87382
    • 10/31/2017 87650
    • 9/9/2017 87669
    • 8/6/2017 88935
    • 11/11/2017 94580
    • 2/18/2017 97848
    • 12/11/2017
Amount recalled
286 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.

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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, 4:46 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.