Reported Oct 26, 2016 · Terminated
Anterior Cervical Fusion Pack, Kit part numbers: AMS2502 and AMS2502(A convenience custom kits used for general surgery…
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?
- Anterior Cervical Fusion Pack
- Kit part numbersAMS2502 and AMS2502(A convenience custom kits used for general surgery in hospital operating room
- Lot codes and dates
- Lot Numbers
- Expiration Dates
6209011/18/20156450311/20/20156516511/9/2015660427/15/2016684969/18/2016757027/4/2017764072/4/2017780602/23/2017786839/8/20177914311/3/2017
- Amount recalled
- 93 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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