Windstone Medical Packaging, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1800-2017)

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:

Vitrectomy Pack, part number AMS4952 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-1800-2017

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: 100 kits

Code Information:

Lot numbers: 84384 85615 96957 99402

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