Z-1796-2017 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
376 kits

Product Description

Plastic Pack, part numbers AMS1028, AMS1028(A, and WAL1189. 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: 76028 76762 77415 77811 80676 81907 82972 83238 84514 86860 88156 89013 89567 94566 95941 97769 98479 99356 101279 102974