Z-3028-2018 Class II Terminated

Recalled by SPS Sterilization, Inc — Nixa, MO

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