Windstone Medical Packaging, Inc. recalls Lasik Tray, part number DDS1045-2 Product packaged in a convenient manner for use in a general clinical procedure

Recalled April 19, 2017 · FDA recall Z-1792-2017 · Windstone Medical Packaging

Hazard

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. · FDA Class II

Units

260 kits

Sold at

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

Description

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.

Product

Lasik Tray, part number DDS1045-2 Product packaged in a convenient manner for use in a general clinical procedure

Manufacturer(s)

Windstone Medical Packaging, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →