Windstone Medical Packaging, Inc.: Medical Device Recall in 2016 - (Recall #: Z-0283-2017)

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:

Vein Kit - No Introducer TVS4027-NI(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-0283-2017

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: 360 kits

Code Information:

Lot Numbers/ Expiration Dates: 60996 8/3/2015 59383 8/20/2015 63706 11/11/2015 65733 11/30/2015 65404 12/26/2015 58253 7/23/2016 58476 8/30/2016 70957 11/6/2016 71370 12/11/2016 72254 1/8/2017 76639 11/19/2017

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