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Recall Observatory FDA recall evidence

Device product

Dr. Landi EVLT Pack, Kit numbers AMS1483(A, AMS1483(B, and AMS1483(C convenience custom kits used for general surgery in hospital operating room

Z-0178-2017

April 22, 2015

Class II

Product summary

Firm
Windstone Medical Packaging, Inc.
Event
Event 71968
Status
Terminated
Classification
Class II
Quantity
2048 kits
Official record key
device-enforcement:Z-0178-2017

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 Numbers/Expiration Dates: 59444 7/10/2014 60056 8/8/2014 60425 8/20/2014 60967 11/3/2014 59000 1/13/2015 63464 2/9/2015 64533 2/25/2015 61267 2/27/2015 63798 3/30/2015 65629 7/30/2015 66813 10/21/2015 69765 11/2/2015 69528 11/18/2015 67138 11/19/2015 67399 1/2/2016 67989 2/6/2016 70374 3/17/2016 69766 3/30/2016 71447 4/18/2016 72241 5/15/2016 57208 7/24/2016 75250 8/7/2016 58621 8/10/2016 73977 8/11/2016 73190 8/12/2016 73277 8/23/2016 74340 8/26/2016 78679 10/24/2016 79046 10/25/2016 75603 1/26/2017 76940 2/11/2017 76159 2/14/2017 78015 6/16/2017 76568 6/26/2017 79824 7/25/2017 81121 8/13/2017 68922

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.