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Recall Observatory FDA recall evidence

Device product

Ophthalmic Pack, Part number WAL1107(A and WAL1190 Product packaged in a convenient manner for use in a general clinical procedure

Z-1794-2017

March 16, 2017

Class II

Product summary

Firm
Windstone Medical Packaging, Inc.
Event
Event 76774
Status
Terminated
Classification
Class II
Quantity
169 packs
Official record key
device-enforcement:Z-1794-2017

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: 87223 88773 89837 95552 97215 97765 100154 100984 102837

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