Windstone Medical Packaging, Inc.: Medical Device Recall in 2016 - (Recall #: Z-0185-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Extremity Tray, Kit number AMS1200(B and AMS1200(C convenience custom kits used for general surgery in hospital operating room

Product Classification:

Class II

Date Initiated: April 22, 2015

Date Posted: October 26, 2016

Recall Number: Z-0185-2017

Event ID: 71968

Reason for Recall:

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.

Status: Terminated

Product Quantity: 816 kits

Code Information:

Lot Numbers/Expiration Dates: 59843 3/1/2015 60753 8/17/2015 59894 9/6/2015 65996 11/13/2015 61600 11/28/2015 62117 12/12/2015 64160 1/3/2016 69211 5/5/2016 56959 6/8/2016 57789 7/1/2016 67355 7/5/2016 58586 8/27/2016 69588 10/8/2016 70509 1/6/2017 72551 1/10/2017 76068 7/17/2017 77502 7/17/2017 78140 9/19/2017

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated