Z-1791-2017 Class II Terminated
Recall Details
- Product Type
- Devices
- Report Date
- April 19, 2017
- Initiation Date
- March 16, 2017
- Termination Date
- June 6, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1,330 kits
Product Description
Eye Pack, part numbers WAL1085(B and WAL1085(C\ Product packaged in a convenient manner for use in a general clinical procedure
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.
Distribution Pattern
Nationwide Distribution including CA, CO, FL, GA, IA, KY, MA, MN, MO, ND, NJ, NV, OH, SD, TX, UT, WI, and WY.
Code Information
Lot numbers: 62736 63388 63389 64189 64190 64586 65070 65171 65307 65714 65715 66342 66343 67079 67080 68165 68166 68234 68641 69264 69536 69545