Z-1790-2017 Class II Terminated

Recalled by Windstone Medical Packaging, Inc. — Billings, MT

Recall Details

Product Type
Devices
Report Date
April 19, 2017
Initiation Date
March 16, 2017
Termination Date
June 6, 2017
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1,520 kits

Product Description

Eye Cataract Pack, part numbers AMS1359 and AMS1359-1 Product packaged in a convenient manner for use in a general clinical procedure

Reason for Recall

AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.

Distribution Pattern

Nationwide Distribution including CA, CO, FL, GA, IA, KY, MA, MN, MO, ND, NJ, NV, OH, SD, TX, UT, WI, and WY.

Code Information

Lot numbers: 62980 63106 63387 63825 63826 64186 64490 64584 65937 75122 75329 77010 77089 77480 77664 78265 78312 78499 79042 79211 79944 79945 80709 80994 82316 82537 82538 82931