Maquet Cardiovascular, LLC: 71 recalls on record

Recalls filed with 1 agency: FDA (71).

First recall on record: January 16, 2013. Most recent: July 22, 2026.

Risk classification: Class I: 3 · Class II: 68

Most recent recalls

DateAgencyProduct
July 22, 2026FDAThe Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI 006075677…Z-2741-2026
October 1, 2025FDAVasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000. The VASOVIE…Z-2636-2025
November 27, 2024FDAAcrobat-i Positioner. Model Number C-XP-5000ZZ-0484-2025
November 27, 2024FDAAcrobat SUV Vacuum Stabilizer System, ST. Model Number C-OM-9000ZZ-0485-2025
November 27, 2024FDAAcrobat-i Vacuum Stabilizer System. Model Number C-OM-10000ZZ-0486-2025
November 6, 2024FDAVasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500Z-0092-2025
July 17, 2024FDAThe VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed for use in conjunc…Z-2338-2024
July 17, 2024FDAThe VASOVIEW HEMOPRO Endoscopic Vessel Harvesting Systems is designed for use in conjunct…Z-2337-2024
July 3, 2024FDAThe VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems are designed for use in conjunc…Z-2176-2024
July 3, 2024FDAThe VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting System, labeled as the following: 1.…Z-2175-2024
January 24, 2024FDAVasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W .Z-0723-2024
January 24, 2024FDAProduct REF 4000-100N, DRAIN, EXPRESS SINGLE W/AC, Single CollectionZ-0709-2024
January 24, 2024FDAProduct REF 4050-100N, DRAIN, EXPRESS BRU W/AC, Blood Recovery UnitZ-0710-2024
January 24, 2024FDAVasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3500.Z-0724-2024
April 12, 2023FDAVASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System, Model Number C-VH-4000Z-1336-2023
April 13, 2022FDAUltima Activator II Reusable Drive Mechanism, part # C-UA-5001. Labeled REF UA-5001.Z-0887-2022
May 13, 2020FDAHEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch, Product Code: M002021758…Z-1871-2020
May 13, 2020FDAHEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch, Product Code: M002021758…Z-1874-2020
May 13, 2020FDAHEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M002021759…Z-1882-2020
May 13, 2020FDAHEMASHIELD PLATINUM Woven Double Velour Vascular Graft-3 Branch, Product Code: M002021759…Z-1876-2020
May 13, 2020FDAHEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Angled 4 Branch, Product Code: M00…Z-1865-2020
May 13, 2020FDAHEMASHIELD PLATINUM Woven Double Velour Vascular Graft01 Branch, Product Code: M002021758…Z-1875-2020
May 13, 2020FDAHemashield Gold Knitted Microvel Double Velour Vascular Graft Axillo-bifemoral, Product C…Z-1861-2020
May 13, 2020FDAHEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175…Z-1869-2020
June 5, 2019FDAMaquet Getinge-BEQ-TOP 5909 1/4 PACK W QPID Material: 701064992Z-1566-2019

Questions about this company

How many recalls does Maquet Cardiovascular, LLC have?
Recalert has 71 U.S. recalls on record for Maquet Cardiovascular, LLC, published between January 16, 2013 and July 22, 2026.
What was the most recent Maquet Cardiovascular, LLC recall?
FDA recall Z-2741-2026, published July 22, 2026: The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI 00607567700406) is a sterile, single-use Class II device that was cleared for marketing by FDA under 510(k) number K101…
Which agencies have handled Maquet Cardiovascular, LLC recalls?
Maquet Cardiovascular, LLC appears as the recalling firm in recalls from: FDA (71).

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