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FDAFDA · Food and drugs·Recall number Z-1328-2017

Lap Pack, part number AMS4801

Published March 8, 2017 · Recall initiated: January 11, 2017

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

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.

What to do

Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Recall details

Manufacturer
Windstone Medical Packaging, Inc.
Distributor
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.
Lot
Lot number and expiration date 88798 4/20/2017 88994 4/16/2017 89895 7/19/2017 97151 7/31/2017
Risk classification
Class II
Area (FDA)
device
Country
United States

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