Recall Z-2080-2025

Edwards Lifesciences, LLC · initiated May 14, 2025

Class I Open, Classified

Class I – dangerous or defective products that could cause serious health problems or death

Product

Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI16 Software Version: N/A Product Description: Cardiac cannula. The Edwards OptiSite Arterial Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours. Component: No.

Codes / lots: Lot Code: Model No:OPTI16; UDI: 00690103180558; All lots up to BSLC9149 Serial Numbers: 130467 130471 130602 130765 130816 130822 130852 130949 131039 131041 131044 131237 131312 131428 131509 131826 131887 131908 132338 132436 132503 132831 BSLC0040 BSLC0165 BSLC0165 BSLC0320 BSLC1309 BSLC1309 BSLC1468 BSLC1468 BSLC1557 BSLC1682 BSLC1688 BSLC1825 BSLC1830 BSLC5302 BSLC5899 BSLC6166 BSLC7142 BSLC7142 BSLC7513 BSLC8176 BSLC8659 BSLC9149

Reason for recall

due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.

FDA-determined cause: Under Investigation by firm

Action taken

On 05/16/2025, and 05/19/2025, the firm sent via FedEx overnight an "URGENT: PRODUCT RECALL" Letter to customers informing them that Edwards has confirmed a small number of occurrences impacting the OptiSite Arterial Perfusion cannula in which a 3mm to 4mm section of wire, from the wire-reinforcement coil at the cannula tip, was found to be released from the cannula body. The risk for the wire-reinforcement coil protruding out of the cannula body is major tissue damage and hemolysis. Customers are instructed to: " Verify their inventory on the attached customer acknowledgement form. " Share this notice with appropriate clinical staff at their site. " No patient follow-up or notification is necessary. " Return a completed Customer Acknowledgment Form to Edwards eCV Representative or via email to Edwards Customer Service at FCA_ECV@edwards.com within 15 days of receipt of this notification. " After receiving RGA number, return any impacted product to Edwards at the address below. A credit will be issued upon receipt of returned product. enableCV Distribution Center 6644 W. 2100 S. Suite D West Valley, UT 84128 For questions/assistance contact - Customer Service at 1-888-943-2783, or email: FCA_ECV@edwards.com

Details

Recall number
Z-2080-2025
Initiated
May 14, 2025
Posted by FDA
July 10, 2025
Product code
DQR – Cannula, Catheter
Quantity
27022
Distribution
Worldwide - US Nationwide distribution including in the states of ALABAMA, ARIZONA, ARKANSAS, CALIFORNIA, COLORADO, CONNECTICUT, DELAWARE, DISTRICT OF COLUMBIA, FLORIDA, GEORGIA, HAWAII, IDAHO, ILLINOIS, INDIANA, IOWA, KANSAS, KENTUCKY, LOUISIANA, MAINE, MARYLAND, MASSACHUSETTS, MICHIGAN, MINNESOTA, MISSISSIPPI, MISSOURI, MONTANA, NEBRASKA, NEVADA, NEW HAMPSHIRE, NEW JERSEY, NEW MEXICO, NEW…
Recalling firm
Edwards Lifesciences, LLC, Irvine, CA

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-2081-2025 Class IBrand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula…due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula… 05/14/2025Open, Classified
Z-2082-2025 Class IBrand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number:…due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula… 05/14/2025Open, Classified
Z-2083-2025 Class IBrand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number:…due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula… 05/14/2025Open, Classified
Z-2084-2025 Class IBrand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number:…due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula… 05/14/2025Open, Classified
Z-2085-2025 Class IBrand Name: FEM-FLEXII Product Name: Femoral Arterial Cannula Model/Catalog Number:…due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula… 05/14/2025Open, Classified