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Recall Observatory FDA recall evidence

Device product

Universal Pack, Kit number AMS2036 convenience custom kits used for general surgery in hospital operating room

Z-0279-2017

April 22, 2015

Class II

Product summary

Firm
Windstone Medical Packaging, Inc.
Event
Event 71968
Status
Terminated
Classification
Class II
Quantity
99 kits
Official record key
device-enforcement:Z-0279-2017

Official wording

Reason: 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.

Code information: Lot Number/ Expiration Date: 63911 6/1/2014 61913 8/10/2014 71796 9/3/2014 68840 9/12/2014 58646 12/17/2014 74391 6/18/2016 78100 6/30/2016

Distribution pattern: Nationwide Distribution to California, Florida, Georgia, Illinois, Kansas, Louisiana, Michigan, New Jersey, Nevada, Texas, Virginia, and Wyoming.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.