Windstone Medical Packaging, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1783-2017)

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:

Cataract Kit, part numbers CAT1467AM and CAT1538(B. 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-1783-2017

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: 4,065 kits

Code Information:

Lot numbers: 76819 76820 78070 78533 78534 78535 79189 79972 80673 80674 80696 81600 82230 83093 83094 83585 83899 84580 85193 86565 86956 87679 88237 88915 88917 89946 95370 95574 95575 96215 96720 97384 97669 99621 99816 99881 101220

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