Windstone Medical Packaging, Inc.: Medical Device Recall in 2016 - (Recall #: Z-0263-2017)

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:

Plastic Pack , Kit number AMS1833(A 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-0263-2017

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: 204 kits

Code Information:

Lot Number/ Expiration Date: 58987 3/10/2014 65124 6/13/2014 63594 6/30/2014 65383 7/3/2014 67936 9/16/2014 68657 9/20/2014 67280 9/27/2014 76180 6/10/2016 57602 6/18/2016 78529 7/30/2016 59242 8/27/2016 80645 11/19/2016

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