Windstone Medical Packaging, Inc.: Medical Device Recall in 2016 - (Recall #: Z-0226-2017)

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:

Lithotomy Pack, Kit number AMS2333 and AMS2333(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-0226-2017

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: 630 kits

Code Information:

Lot numbers/Expiration dates: 61276 3/4/2014 61277 3/10/2014 62761 11/15/2015 64641 11/30/2015 65276 11/30/2015 69772 12/3/2015 71457 12/3/2015 68312 12/5/2015 69392 12/17/2015 71152 12/17/2015 68629 12/25/2015 64905 12/27/2015

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