Z-3028-2018 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
- 6 units total
Product Description
Edwards Lifesciences EZ Glide Aortic Cannula, 24F x 37.6CM, 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 EZC24A-R; Lot Number 59634962; Serial Numbers 16401032017-01, 16401032017-02, 16401032017-03, 16401032017-04, 16401032017-05, 16401032017-06, 16401032017-07, 16401032017-08, 16401032017-09, 16401032017-10, 16401032017-11, 16401032017-12, 16401032017-13, 16401032017-14, 16401032017-15, 16401032017-16, 16401032017-17, 16401032017-18, 16401032017-19, 16401032017-20, 16401032017-21, 16401032017-22, 16401032017-23, 16401032017-24, 16401032017-25, 16401032017-26, 16401032017-27, 16401032017-28, 16401032017-29, 16401032017-30, 16401032017-31, 16401032017-32, 16401032017-33, 16401032017-34, 16401032017-35, 16401032017-36, 16401032017-37