RecallDepth

Lap Band Pack, part number AMS1785(A

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-1324-2017
Quantity
252 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  85157, 2/28/2017 86861, 2/28/2017 87419, 4/30/2017 88367, 3/31/2017 89154, 7/31/2017 94568, 7/31/2017 94919, 11/30/2017 95972, 10/31/2017 96744, 11/30/2017 97772, 11/30/2017 98016, 11/30/2017 98495, 3/31/2018

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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