Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of GetingeLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Maquet Cardiovascular with 252 device recalls and 14 510(k) clearances. The most recent is a device recall dated Jun 2, 2026: The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI 00607567….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jun 2, 2026 | The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI 00607567700406) is a sterile, single-use Class II device thaClass II · Getinge identified that Vasoview Hemopro 2 devices from Lot 3000547797 were exposed to an out-of-specification steriliza | Device recalls |
| Apr 27, 2026 | Fusion Bioline Vascular GraftK252445 · DSY | 510(k) clearances |
| Aug 15, 2025 | Heartstring III Proximal Seal System. Intravascular anastomosis occluder.Class II · Three failure modes have been identified: failure of the Heartstring Seal to load, failure of the Heartstring Seal to de | Device recalls |
| Aug 15, 2025 | Heartstring III Proximal Seal System, 3.8 MM. Intravascular anastomosis occluder.Class II · Three failure modes have been identified: failure of the Heartstring Seal to load, failure of the Heartstring Seal to de | Device recalls |
| Aug 15, 2025 | Heartstring III Proximal Seal System, 4.3 MM. Intravascular anastomosis occluder.Class II · Three failure modes have been identified: failure of the Heartstring Seal to load, failure of the Heartstring Seal to de | Device recalls |
| Aug 6, 2025 | Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000. The VASOVIEW HEMOPRO 3 Endoscopic Vessel Harvesting (EVH) SystClass II · Reports of out-of-box failures discovered during the limited launch phase. Failure modes included angled deformity at th | Device recalls |
| May 30, 2025 | Vasoview Hemopro 3 Endoscopic Vessel Harvesting System (VH-6000); Vasoview Hemopro 3 Endoscopic Vessel Harvesting System with Vasoshield (VH-6001); Vasoview Hemopro 3 Power Supply (VH-6010)K251238 · GEI | 510(k) clearances |
| Mar 20, 2025 | The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed for use in conjunction with the 7 mm extended length endoscope. The HClass II · There have been at least 12 complaints from users as of March 3, 2025, reporting that they identified the ceramic C-Ring | Device recalls |
| Mar 10, 2025 | Maquet VH-3010 Power Supply. Used to deliver power to the harvesting tool of the Vasoview Hemopro EVH System (HemoPro 2).Class II · Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the jaws of the HemoPro 2 to not adequately hea | Device recalls |
| Feb 26, 2025 | Vasoview Hemopro 3 Power SupplyK243918 · GEI | 510(k) clearances |
| Dec 9, 2024 | VasoView HemoPro 2 Endoscopic Vessel Harvesting System. Model Numbers: VH-4000. Indicated for use in minimally invasive surgery allowing acClass I · Potential for two issues: 1. Bent or detached heater wire; 2. Silicone peeling or detaching from the Jaws of the Harv | Device recalls |
| Feb 27, 2024 | Vasoview Hemopro 3 Endoscopic Vessel Harvesting System (VH-6000), Vasoview Hemopro 3 Endoscopic Vessel Harvesting System with Vasoshield (VH-6001), Vasoview Hemopro 3 Power Adapter (VH-6020)K233879 · GEI | 510(k) clearances |
| Apr 15, 2020 | 7 mm Extended Length EndoscopeK191930 · GCJ | 510(k) clearances |
| Sep 17, 2019 | VASOVIEW HEMOPRO Extension Cable, VASOVIEW HEMOPRO 2 Extension Cable, Bipolar Extension Cable, Fixed Distance, Active Return CordK191947 · GEI | 510(k) clearances |
| Apr 19, 2016 | VASOVIEW HemoPro Endoscopic Vessel Harvesting SystemK153194 · GEI | 510(k) clearances |
| Feb 16, 2016 | FUSION Vascular GraftK153523 · DSY | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
