Z-3027-2018 Class II Terminated
Recall Details
- Product Type
- Devices
- Report Date
- September 19, 2018
- Initiation Date
- March 7, 2018
- Termination Date
- November 27, 2018
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 10 units total
Product Description
Edwards Lifesciences Aortic Perfusion Cannula, 24F x 30CM, resterilized.
Reason for Recall
The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.
Distribution Pattern
US distribution to AZ, CA, FL, OH, PA, TX, VA, WV
Code Information
Code Number AAO24TFA-R; Lot Number 59736014; Serial Numbers 16504192017-01, 16504192017-02, 16504192017-03, 16504192017-04, 16504192017-05, 16504192017-06, 16504192017-07, 16504192017-08, 16504192017-09, 16504192017-10