Reported Oct 26, 2016 · Terminated
Extremity Pack, Kit number AMS2726, AMS2937, AMS3240, PSS1381(A PSS1381(B, PSS1798(A, PSS1842(A, and PSS2706…
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?
- Extremity Pack, Kit number AMS2726, AMS2937, AMS3240, PSS1381(A PSS1381(B, PSS1798(A, PSS1842(A, and PSS2706 convenience custom kits used for general surgery in hospital operating room
- Lot codes and dates
- Lot Numbers/Expiration Dates
230 of 230 codes
599265/26/2014606688/14/2014703101/17/2015686661/20/2015627451/29/2015698362/9/2015666614/25/2015595867/22/2015602647/23/2015592048/5/2015613828/20/2015630639/4/2015610129/11/2015610139/14/20156481710/10/20156161810/15/20156138310/18/20156459310/19/20156496911/3/20156577611/5/20156439411/14/20156377811/15/20156558011/16/20156193811/17/20156256711/18/20156162611/20/20156691711/21/20156134311/22/20156639311/23/20156215411/23/2015
- Lot Numbers/Expiration Dates
- Amount recalled
- 3829 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.
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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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