FDA Recall Open, Classified

(1) CryoPatch SG Pulmonary Human Cardiac Hemi-Artery - Artery Patch, SGPH00 Cryopreserved Decellularized Cardiac Tissue Allograft Prepared with SynerGraft (SG) Technology; and (2) CryoPatch SG Pulmonary Human Cardiac Branch Patch, SGP020, Cryopreserved Decellularized Cardiac Tissue Allograft Prepared with SynerGraft (SG) Technology.

Recall: Z-2532-2024 · Initiated May 28, 2024

Recall

Recall Number
Z-2532-2024
Event Number
94909
Firm
Artivion, Inc
FEI Number
3001451326
Product Code
DXZ
Status
Open, Classified
Root Cause
Under Investigation by firm
Initiated
May 28, 2024
Posted
August 8, 2024
Address
1655 Roberts Blvd Nw, Kennesaw, GA, 30144-3632

Description

(1) CryoPatch SG Pulmonary Human Cardiac Hemi-Artery - Artery Patch, SGPH00 Cryopreserved Decellularized Cardiac Tissue Allograft Prepared with SynerGraft (SG) Technology; and (2) CryoPatch SG Pulmonary Human Cardiac Branch Patch, SGP020, Cryopreserved Decellularized Cardiac Tissue Allograft Prepared with SynerGraft (SG) Technology.

Reason

Grafts were found to have been approved, released, shipped and implanted with an invalid test results.

Action

The recalling firm issued letters to their Field Representatives on 5/24/2024 or 5/28/2024 for distribution to the consignees via email or hand delivery. The first date consignees were notified was on 5/28/2024 by their Field Representative. The letter provided the details on the tissue the consignee received, the date it was implanted, and the implanting surgeon. The issue was described and it was pointed out there was no indication the impacted tissues were contaminated and unlikely to pose a health risk to the patient. The letter discussed the testing conducted on each allograft and that the identified allograft was reported to have an invalid Post-Processing Sterility test result or a Pre-Processing Culture test result (depending on the consignee letter), which represents a technical failure in the test, not an indication of a positive result. A response form was enclosed for return to acknowledge receipt of the notification.

Distribution

US Nationwide distribution in the states of CA, DC, FL, and NY.

Quantity

2 arteries, 1 patch