Windstone Medical Packaging, Inc.: Medical Device Recall in 2016 - (Recall #: Z-0146-2017)

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:

Basic Kit, Part numbers BP1110(C and CMP1109(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-0146-2017

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: 53 kits

Code Information:

Lot Numbers/Expiration Dates: 57495 7/3/2016 57946 6/29/2016 59013 8/22/2016 59014 3/28/2015 60496 9/1/2015 61879 11/6/2015 62950 11/28/2015 64294 1/7/2016 65396 11/3/2015 65981 11/1/2015 67215 7/16/2016 68373 9/4/2016 70215 9/15/2016 71010 10/17/2016 72059 3/21/2017 73446 3/7/2017 73960 4/5/2017 74662 5/9/2017 75137 5/5/2017 75760 7/13/2017 77133 7/17/2017 77727 8/16/2017 78449 9/15/2017 79367 1/25/2018 79939 1/17/2018

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