Windstone Medical Packaging, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1380-2017)

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:

Vascular Pack, part number AMS4030 Vascular Pack, part number AMS4030(A

Product Classification:

Class II

Date Initiated: January 11, 2017

Date Posted: March 8, 2017

Recall Number: Z-1380-2017

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: 360 kits

Code Information:

Lot number and expiration date 89251, 12/25/2018 89524, 10/25/2018 89601, 12/17/2018 89838, 12/17/2018 99349, 6/18/2019 99729, 10/7/2019

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