Windstone Medical Packaging, Inc.: Medical Device Recall in 2016 - (Recall #: Z-0279-2017)

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:

Universal Pack, Kit number AMS2036 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-0279-2017

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: 99 kits

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.

Voluntary or Mandated:

Voluntary: Firm initiated