Windstone Medical Packaging, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1784-2017)

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 - Dr. Slingsby, part number CMP1017(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-1784-2017

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: 990 kits

Code Information:

Lot numbers: 77429 79999 81143 81960 84055 84556 85169 85550 86501 87632 87819 96056 96963 97873 98741 99416 99763 100278 101449

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