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Artivion, Inc: Medical Device Recalls in 2024

Updated on March 25, 2026.

According to to data from the FDA, there were 3 medical device recalls made by Artivion, Inc in 2024. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.
See this for other years:
2024
  • (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.
  • CryoValve SG Pulmonary Human Heart Valve, SGPV00, Cryopreserved Decellularized Heart Valve Allograft Prepared with SynerGraft (SG) Technology.
  • CryoValve SG Cryopreserved Pulmonary Human Heart Valve
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