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Recall Observatory FDA recall evidence

Device product

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

Z-1792-2017

March 16, 2017

Class II

Product summary

Firm
Windstone Medical Packaging, Inc.
Event
Event 76774
Status
Terminated
Classification
Class II
Quantity
260 kits
Official record key
device-enforcement:Z-1792-2017

Official wording

Reason: 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.

Code information: Lot numbers: 100960 103358 79099 81317 82664 82900 85028 86965 88297 89067 89311 94809 95531 98618 99932

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

Derived failure modes

  • Sterility assurance

    reason.sterility_assurance · v1.0.0

    sterile packaging of the eye pad to be compromised