FDAFDA · Food and drugs·Recall number Z-0252-2017
Open Procedure Pack II, Kit number RMS1740(A convenience custom kits used for general surgery in hospital operating room
Published October 26, 2016 · Recall initiated: April 22, 2015
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Windstone Medical Packaging, Inc.
- Distributor
- Nationwide Distribution to California, Florida, Georgia, Illinois, Kansas, Louisiana, Michigan, New Jersey, Nevada, Texas, Virginia, and Wyoming.
- Lot
- Lot Numbers/ Expiration Dates: 59942 4/3/2015 59692 4/19/2015 59858 11/25/2015 65398 11/30/2015 66543 7/4/2016 67496 9/14/2016 70943 1/31/2017 70944 8/11/2017 79014 9/17/2017 79771 1/10/2018
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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