Artivion, Inc recall records

3 reported ongoing

3 records in this archive. Latest source date May 28, 2024.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

Records and reported status

FDA device enforcement

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

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

Class IIReported ongoing

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

Official source for (1) CryoPatch SG Pulmonary Human Cardiac Hemi-Artery - Artery Patch, SGPH00 Cryopreserved Decellu...

Reasons in these listed records

  • Grafts were found to have been approved, released, shipped and implanted with an invalid test results.
  • The blood cultures performed as part of the organ donation process were positive for Staphylococcus aureus.

These examples come from this result page and are not a ranking of every recall reason.

Checking Artivion, Inc

Is there a recall on artivion, inc right now?

This archive contains 3 records, including 3 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

How do I check my package or product?

Compare the product, firm and lot, date, model or serial identifiers with the notice. Use the label-check guide if you need help locating an identifier.

Does a matching name mean every item is included?

A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.

What if the search finds no matching record?

This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. Check source coverage and the agency's current notices.

Where can I find older records?

Use monthly archives or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

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