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Artivion, Inc
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Type Company Card addedAugust 10 Threat lists flagged Reviews1
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Threat lists · flagged Product safety recall
Official safety regulators published alerts about a product of this kind.
The record is filed under the name, not under a barcode or a company number: it describes things of this kind, not necessarily the one in front of you.
Alerts on record3 HazardGrafts were found to have been approved, released, shipped and implanted with an invalid test results. First alertMarch 6, 2024 Latest alertMay 28, 2024 On our lists sinceAugust 10, 2026
What to do: Check the maker, the batch and the date of the exact item you have — the alert is about this kind of product.
Where this came from: openFDA device recalls — An official government safety register — product recalls and safety alerts.
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Reviews · 1
Artivion, Inc. is a cardiovascular and aortic medical-device company, so its work belongs in operating rooms rather than on a pharmacy shelf. By our assessment, the strong point is clear specialization: this is the sort of business that focuses on life-supporting, high-stakes surgical tools and implants, where precision matters more than breadth. The downside is just as clear, because a company tied to complex procedures depends on hospital adoption, surgeon training, and regulatory scrutiny. In practice, that usually means grafts, repair products, and devices used when the anatomy is unforgiving and there is no room for sloppy design. It sits in the more serious end of medtech, alongside other cardiovascular specialists, not alongside general-purpose healthcare brands. People who want a dedicated name in heart and vascular surgery will understand the point of Artivion, while anyone looking for a broad consumer health company will not. By our assessment, it earns a solid mark for focus and for operating in a field where that focus matters.
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