Windstone Medical Packaging, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1315-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Hernia Pack, part number AMS3859

Product Classification:

Class II

Date Initiated: January 11, 2017

Date Posted: March 8, 2017

Recall Number: Z-1315-2017

Event ID: 76280

Reason for Recall:

The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility.

Status: Terminated

Product Quantity: 228 kits

Code Information:

Lot number and expiration date 101167, 5/30/2019 87349, 6/20/2018 88830, 9/11/2018 89510, 11/29/2018 94616, 11/15/2018 94704, 11/24/2018 95209,11/25/2018 95934, 1/15/2019 97409, 3/6/2019 99486, 3/12/2019

Distribution Pattern:

Distributed in AZ, CA, CO, CT, FL, GA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NJ, NV, OH, PA, TX, UT, VA, and WA.

Voluntary or Mandated:

Voluntary: Firm initiated