Reported Mar 8, 2017 · Terminated
Hernia Pack, part number AMS3859
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?
- Hernia Pack, part number AMS3859
- Lot codes and dates
Lot number and expiration date 1011675/30/2019 873496/20/2018 888309/11/2018 8951011/29/2018 9461611/15/2018 9470411/24/2018 9520911/25/2018 959341/15/2019 974093/6/2019 994863/12/2019
- Amount recalled
- 228 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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