Windstone Medical Packaging, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1796-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Plastic Pack, part numbers AMS1028, AMS1028(A, and WAL1189. Product packaged in a convenient manner for use in a general clinical procedure

Product Classification:

Class II

Date Initiated: March 16, 2017

Date Posted: April 19, 2017

Recall Number: Z-1796-2017

Event ID: 76774

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.

Status: Terminated

Product Quantity: 376 kits

Code Information:

Lot numbers: 76028 76762 77415 77811 80676 81907 82972 83238 84514 86860 88156 89013 89567 94566 95941 97769 98479 99356 101279 102974

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated