Windstone Medical Packaging, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1791-2017)

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:

Eye Pack, part numbers WAL1085(B and WAL1085(C\ 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-1791-2017

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: 1,330 kits

Code Information:

Lot numbers: 62736 63388 63389 64189 64190 64586 65070 65171 65307 65714 65715 66342 66343 67079 67080 68165 68166 68234 68641 69264 69536 69545

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