Maquet Cardiovascular recalls

Maquet Cardiovascular has 252 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 22 Jul 2026. 35 are still ongoing. 5 were reported in the last 12 months. The most frequent reason is sterility.

Total recalls252since 2013

Last 12 months5reported

Class I52% of total

Ongoing35latest 22 Jul 2026

Recalls per month, last 24 months

click a bar for that month

0Oct '24 4 0 2Jan '25 0 0 2Apr 0 0 0Jul 0 3 1Oct 0 0 0Jan '26 0 0 0Apr 0 0 1Jul 0 0

Severity split

Class I 5 2%Class II 247 98%Class III 0 0%

Why maquet cardiovascular is recalled

Product types

By year

202610%
202583%
2024125%
2023135%
202231%
202110%
20202410%
201918473%
201710%
201410%

Ongoing maquet cardiovascular recalls

35 active

Reported	Class	Recall	Company	Reason	Where
22 Jul 2026Device	CLASS II	The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System recalled	Maquet Cardiovascular	Sterility	Nationwide
1 Oct 2025Device	CLASS II	Vasoview Hemopro 3 Endoscopic Vessel Harvesting System recalled	Maquet Cardiovascular	Device Malfunction	Nationwide
24 Sep 2025Device	CLASS II	Heartstring III Proximal Seal System Intravascular recalled	Maquet Cardiovascular	Packaging Defects	Nationwide
24 Sep 2025Device	CLASS II	Heartstring III Proximal Seal System Intravascular recalled	Maquet Cardiovascular	Packaging Defects	Nationwide
24 Sep 2025Device	CLASS II	Heartstring III Proximal Seal System recalled by Maquet Cardiovascular	Maquet Cardiovascular	Packaging Defects	Nationwide
30 Apr 2025Device	CLASS II	The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System recalled	Maquet Cardiovascular	Device Malfunction	Nationwide

All maquet cardiovascular recalls, newest first

252 total

Reported	Class	Recall	Company	Reason	Where
22 Jul 2026Device	CLASS II	The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System recalled	Maquet Cardiovascular	Sterility	Nationwide
1 Oct 2025Device	CLASS II	Vasoview Hemopro 3 Endoscopic Vessel Harvesting System recalled	Maquet Cardiovascular	Device Malfunction	Nationwide
24 Sep 2025Device	CLASS II	Heartstring III Proximal Seal System Intravascular recalled	Maquet Cardiovascular	Packaging Defects	Nationwide
24 Sep 2025Device	CLASS II	Heartstring III Proximal Seal System Intravascular recalled	Maquet Cardiovascular	Packaging Defects	Nationwide
24 Sep 2025Device	CLASS II	Heartstring III Proximal Seal System recalled by Maquet Cardiovascular	Maquet Cardiovascular	Packaging Defects	Nationwide
30 Apr 2025Device	CLASS II	The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System recalled	Maquet Cardiovascular	Device Malfunction	Nationwide
23 Apr 2025Device	CLASS II	Maquet VH-3010 Power Supply recalled by Maquet Cardiovascular	Maquet Cardiovascular	Other	Nationwide
15 Jan 2025Device	CLASS I	Vasoview Hemopro 2 (w/Vasoshield) Endoscopic Vessel recalled	Maquet Cardiovascular	Other	Nationwide
15 Jan 2025Device	CLASS I	VasoView HemoPro 2 Endoscopic Vessel Harvesting System recalled	Maquet Cardiovascular	Other	Nationwide
27 Nov 2024Device	CLASS II	Acrobat-i Positioner recalled by Maquet Cardiovascular	Maquet Cardiovascular	Sterility	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.