—#152834

Product

Dr. Landi EVLT Pack, part number AMS1483(E Dr. Landi EVLT Pack, part number AMS1483(E

FDA product code: FSY — Light, Surgical, Ceiling Mounted
Device class: Class 2
Medical specialty: General, Plastic Surgery
Affected lot / code info: Lot number and expiration date 100007, 2/26/2019 100008, 2/3/2019 100009, 2/10/2019 100322, 4/2/2019 101129, 2/21/2019 84854, 12/26/2017 85111, 12/1/2017 86047, 12/19/2017 86791, 5/7/2018 88616, 5/13/2018 88617, 6/11/2018 88845, 6/12/2018 89076, 10/22/2018 89175, 10/7/2018 89568, 11/9/2018 89715, 11/25/2018 94567, 10/23/2018 97120, 12/7/2018 97562, 11/27/2018 97771, 11/27/2018 98014, 11/11/2018 98014, 11/11/2018 98160, 2/22/2018 98161, 11/21/2018 98162, 11/30/2018 98494, 2/13/2019

Why it was recalled

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.

Root cause (FDA determination)

Nonconforming Material/Component

Action the firm took

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.

Recalling firm

Firm: Windstone Medical Packaging, Inc.
Address: 1602 4th Ave N, Billings, Montana 59101-1521

Distribution

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.

Timeline

Recall initiated: 2017-01-11
Posted by FDA: 2017-02-28
Terminated: 2017-05-03
Status: —

Source: openFDA Device Recall endpoint. Recall record ID #152834. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.