Windstone Medical Packaging, Inc.: Medical Device Recall in 2016 - (Recall #: Z-0229-2017)

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:

Lumbar Laminectomy Pack, Kit number AMS2501 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-0229-2017

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: 249 kits

Code Information:

Lot numbers/Expiration dates: 64906 11/3/2015 66041 11/6/2015 62111 11/12/2015 65892 12/22/2015 66759 7/29/2016 69271 9/19/2016 68960 9/26/2016 67958 9/28/2016 70334 1/29/2017 74063 5/15/2017 75454 7/8/2017 80958 8/8/2017 78464 9/14/2017 77100 10/25/2017 79659 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