Artivion recalls

Artivion has 3 recalls on record with the FDA and USDA, the earliest in 2024 and the latest reported on 14 Aug 2024. 3 are still ongoing.

Total recalls3since 2024

Last 12 months0reported

Class I00% of total

Ongoing3latest 14 Aug 2024

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 3 100%Class III 0 0%

Why artivion is recalled

Other Reasons3100%

Product types

Heart & Vascular Devices267%
Other Medical Devices133%

By year

20243100%

Ongoing artivion recalls

3 active

Reported	Class	Recall	Company	Reason	Where
14 Aug 2024Device	CLASS II	CryoValve SG Pulmonary Human Heart Valve, SGPV00 recalled by Artivion	Artivion	Other	Nationwide
14 Aug 2024Device	CLASS II	CryoPatch SG Pulmonary Human Cardiac Hemi-Artery recalled by Artivion	Artivion	Other	Nationwide
24 Apr 2024Device	CLASS II	CryoValve SG Cryopreserved Pulmonary Human Heart Valve recalled	Artivion	Other	Nationwide

All artivion recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
14 Aug 2024Device	CLASS II	CryoValve SG Pulmonary Human Heart Valve, SGPV00 recalled by Artivion	Artivion	Other	Nationwide
14 Aug 2024Device	CLASS II	CryoPatch SG Pulmonary Human Cardiac Hemi-Artery recalled by Artivion	Artivion	Other	Nationwide
24 Apr 2024Device	CLASS II	CryoValve SG Cryopreserved Pulmonary Human Heart Valve recalled	Artivion	Other	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.