RecallDepth

Plastic Kit, part number CMP1084(C

This recall has been terminated (originally issued February 28, 2017).

Company
Windstone Medical Packaging, Inc.
Recall Initiated
January 11, 2017
Posted
February 28, 2017
Terminated
May 3, 2017
Recall Number
Z-1360-2017
Quantity
580 kits
Firm Location
Billings, MT
Official Source
View on FDA website ↗

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.

Distribution

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 / Code Info

Lot number and expiration date  86626, 9/3/2017 87202, 9/16/2017 87481, 9/9/2017 87924, 9/17/2017 88217, 10/31/2017 88819, 10/27/2017 89271, 10/11/2017 89539, 12/7/2017 95831, 1/9/2018 96460, 4/12/2018 98055, 6/30/2018 98962, 6/22/2018 99088, 9/15/2018

Root Cause

Nonconforming Material/Component

Action Taken

AMS notified their consignees by Email, Fax, and Phone on 11/11/2017. AMS sent the notification letter, dated January 11, 2017, and provided yellow stickers "Recall Notice" to customers. They are advised to over-label the affected AMS kits at their facilities. Customers were instructed to place sticker in such a way that it would be immediately noticed but should not cover up or conceal any pertinent information such as Pack Number, Pack Name, Lot Number or Expiration Date on a kit. Customers with questions can call Vicki Davis at 321-527-7714 or send email to vdavis@alignedmedicalsolutions.com.

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