Maquet Cardiovascular, LLC recalls
Every recall we track for Maquet Cardiovascular, LLC — 246 in all, from 2019–2026 — plus the complaints and injury reports the public filed about them. 15 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Maquet Cardiovascular, LLC peaked in 2019 (184); 246 since 2017. 6% rated “stop using now”.
All FDA recall records for Maquet Cardiovascular, LLC since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 1 | 13 | 152 | 18 | 184 |
| 2020 | 13 | 7 | 1 | 3 | 24 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 2 | 2 | 1 | 5 |
| 2023 | 0 | 10 | 3 | 2 | 15 |
| 2024 | 0 | 4 | 6 | 0 | 10 |
| 2025 | 1 | 2 | 1 | 2 | 6 |
| 2026 (to date) | 0 | 0 | 0 | 1 | 1 |
What to do if you have a recalled Maquet Cardiovascular, LLC product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Maquet Cardiovascular, LLC recalls
26 shown- UnratedMedical device
Maquet Cardiovascular, LLC recalls The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI 00607567700406) is a sterile, single-use
Recall of Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000) with Lot 3000547797 due to potential exposure to improper sterilization during gamma processing.
Maquet CardiovascularJun 2, 2026 - UnratedMedical device
Maquet Cardiovascular, LLC recalls Heartstring III Proximal Seal System. Intravascular anastomosis occluder.
Maquet recalls Heartstring III Proximal Seal System for potential bleeding during surgery. Affected units have specific serial numbers and model numbers. Contact for return or replacement.
MaquetAug 15, 2025 - Use cautionMedical device
Maquet Cardiovascular, LLC recalls Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000. The VASOVIEW HEMOPRO 3 Endoscopic Vessel
Maquet recalls Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model C-VH-6000 due to out-of-box failures including angled deformity, jaws not fully closed, and heater wire issues. Affected units sold during limited launch phase.
Maquet CardiovascularAug 6, 2025 - Use cautionMedical device
Maquet Cardiovascular, LLC recalls The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed for use in conjunction with the 7 mm extended
Maquet recalls VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting Systems with broken ceramic C-Rings. 12 complaints reported by March 3, 2025. Affected units manufactured Nov 5, 2024 - Feb 14, 2025.
MaquetMar 20, 2025 - Lower riskMedical device
Maquet Cardiovascular, LLC recalls Maquet VH-3010 Power Supply. Used to deliver power to the harvesting tool of the Vasoview Hemopro EVH System (HemoPro
Maquet recalls VH-3010 Power Supply units that may cause HemoPro 2 harvesting tool to fail to heat properly due to incorrect resistor use. Affected units have specific serial numbers.
MaquetMar 10, 2025 - Use cautionMedical device
Maquet Cardiovascular, LLC recalls VasoView HemoPro 2 Endoscopic Vessel Harvesting System. Model Numbers: VH-4000. Indicated for use in minimally invasive
Maquet recalls VasoView HemoPro 2 Endoscopic Vessel Harvesting System (model VH-400: 00607567700406) due to potential heater wire detachment or silicone peeling. Affected units may cause injury during minimally invasive surgery.
MaquetDec 9, 2024 - Lower riskMedical device
Maquet Cardiovascular, LLC recalls Acrobat-i Vacuum Stabilizer System. Model Number C-OM-10000Z
Maquet recalls Acrobat-i Vacuum Stabilizer System (model C-OM-10000Z) due to potential sterility compromise after 2 years. Affected units have specific batch numbers. Consumers should check their product for batch numbers and contact Maquet for details.
MaquetOct 16, 2024 - Lower riskMedical device
Maquet Cardiovascular, LLC recalls VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500
Maquet recalls VasoView HemoPro Endoscopic Vessel Harvesting System (product codes VH-3000-W and VH-3500) due to reports of silicone detaching from the Harvesting Tool during use. Affected units have specific lot numbers and product codes.
MaquetSep 20, 2024 - Lower riskMedical device
Maquet Cardiovascular, LLC recalls The VASOVIEW HEMOPRO Endoscopic Vessel Harvesting Systems is designed for use in conjunction with the 7 mm Extended
Maquet recalls VASOVIEW HEMOPRO Endoscopic Vessel Harvesting Systems with potential C-Ring wire straightening due to insufficient bend radius, affecting 27 complaints between March and April 2024. No injuries reported.
MaquetMay 31, 2024 - Use cautionMedical device
Maquet Cardiovascular, LLC recalls The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting System, labeled as the following: 1. VasoView Hemopro 2, Model
Maquet recalls VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting Systems (models VH-4000/VH-4001) due to potential fluid ingress causing improper cautery function. Affected units may not provide intended cauterization or cause unintended burns during surgery.
MaquetMay 17, 2024 - Use cautionMedical device
Maquet Cardiovascular, LLC recalls Product REF 4050-100N, DRAIN, EXPRESS BRU W/AC, Blood Recovery Unit
Maquet recalls blood recovery units with pre-packaged sterile water syringes that may cause infection if not kept upright. Affected units have specific lot numbers and serial codes.
MaquetDec 13, 2023 - Lower riskMedical device
Maquet Cardiovascular, LLC recalls Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W .
Maquet recalls Vasoview Hemopro Endoscopic Vessel Harvesting System model VH-3000-W due to potential polyimide particles entering arterial grafts during coronary or peripheral bypass surgery.
Maquet CardiovascularDec 1, 2023 - Use cautionMedical device
Maquet Cardiovascular, LLC recalls Acrobat-i Vacuum Positioner System, Model Number XP-5000Z
Maquet recalls Acrobat-i Vacuum Positioner System model XP-5000Z due to positioner arm not tightening or locking during use. Affected units have specific lot numbers and UDI-DI codes.
MaquetOct 31, 2023 - Lower riskMedical device
Maquet Cardiovascular, LLC recalls Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System, Model VH-2400 printed on outer label, inner label and IFU,
Maquet recalls Vasoview 6 Pro (VV6) endoscopic vessel harvesting system with incorrect box artwork that could lead to confusion about the device model.
Maquet CardiovascularSep 19, 2023 - Use cautionMedical device
Maquet Cardiovascular, LLC recalls Maquet Acrobat-i Vacuum Stabilizer System Intended for use during performance of cardiac surgical procedures through a
Maquet recalls Acrobat-i Vacuum Stabilizer Systems with risk of housing mount jaw breaking during cardiac surgery, potentially causing injury to heart tissue or blood vessels. Affected units have specific product codes and lot numbers.
MaquetSep 13, 2023 - Use cautionMedical device
Maquet Cardiovascular, LLC recalls ACROBAT SUV Vacuum Off-Pump System, Part Number C-OM-9000S. Component of a chest stabilization system for cardiac and
Maquet recalls ACROBAT SUV Vacuum Off-Pump System (part C-OM-90:000S) due to potential instability during cardiac surgery, risking device failure and patient safety.
MaquetJun 28, 2023 - UnratedMedical device
Maquet Cardiovascular, LLC recalls VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System, Model Number C-VH-4000
Maquet recalls VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System (model C-VH-4000) due to unsterilized batches. Affected units have specific lot numbers. Consumers should contact Maquet for details.
MaquetMar 6, 2023 - Use cautionMedical device
Maquet Cardiovascular, LLC recalls Fusion Bioline Vascular Graft, Part number M00201503046B0
Maquet recalls Fusion Bioline Vascular Grafts from specific lot numbers due to potential reduced blood flow or bleeding risks. Affected units may cause pseudo-aneurysms if used improperly.
MaquetJan 30, 2023 - Use cautionMedical device
Maquet Cardiovascular, LLC recalls Vasoshield Syringe Packs, Model VH-5001
Maquet recalls Vasoshield syringe packs with model VH-5001 due to potential ink chip causing patient harm. Affected units have specific serial numbers and UDI-DI codes.
MaquetDec 22, 2022 - UnratedMedical device
Maquet Cardiovascular, LLC recalls INTERGARD Woven Vascular Graft is a woven polyester graft coated with a bovine collagen. It has an external velour
Maquet recalls Intergard Woven Vascular Grafts labeled as 8mm x 30cm but actually 32mm x 30cm. This mislabeling could lead to improper use in medical procedures.
MaquetApr 29, 2022 - Lower riskMedical device
Maquet Cardiovascular, LLC recalls Ultima Activator II Reusable Drive Mechanism, part # C-UA-5001. Labeled REF UA-5001.
Maquet recalls Ultima Activator II Reusable Drive Mechanism part # C-UA-5001 due to potential corrosion causing allergic reactions and metal toxicity. Affected lots: 25153700, 25157489, 25158616.
MaquetFeb 9, 2022 - Lower riskMedical device
Maquet Cardiovascular, LLC recalls HEMASHIELD GOLD KNITTED MICROVEL DOUBLE VELOUR VASCULAR GRAFT- D: 7 mm; L: 60 cm Indicated for use in the replacement
Maquet recalls HEMASHIELD Gold vascular grafts with mismatched labeling that could disrupt blood vessel repairs, risking pseudo-aneurysms. Affected units have specific size and lot numbers.
MaquetJan 14, 2022 - Lower riskMedical device
Maquet Cardiovascular, LLC recalls Hemashield Gold Knitted Bifurcated, 18 mm x 9 mm; reference number M002020851890
Maquet recalls Hemashield Gold Knitted Bifurcated Vascular Grafts (18mm x 9mm) due to probable mislabeling with Platinum models. Affected units may contain incorrect product specifications.
MaquetDec 1, 2021 - Use cautionMedical device
Maquet Cardiovascular, LLC recalls HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-3 Branch, Product Code: M00202175912P0 - Product Usage: for use
Maquet recalls Hemashield Platinum Woven Double Velour Vascular Grafts with potential small holes at seam lines causing bleeding during surgery. Affected units have specific serial numbers.
MaquetApr 7, 2020 - Lower riskMedical device
Maquet Cardiovascular, LLC recalls Maquet Getinge-BEQ-TOP 5502 ECC Pack Material:701051791R01
Maquet recalls Getinge-BEQ-TOP 5502 ECC packs with batch numbers 3000074733 and 3000081599 due to potential sterility issues after sterilization.
MaquetApr 18, 2019 - Lower riskMedical device
Maquet Cardiovascular, LLC recalls AXIUS Blower Mister Product Code/REF Number: CB-1000 The Axius Blower Mister is intended to clear an anastomotic site
Maquet recalls Axius Blower Mister (CB-1000) due to potential CO2 flow issues during off-pump coronary artery bypass surgery. Affected units have specific lot numbers; contact for remedy.
MaquetJan 24, 2019
Maquet Cardiovascular, LLC recall questions
How many recalls has Maquet Cardiovascular, LLC had?
246 recalls from Maquet Cardiovascular, LLC are on record with U.S. safety agencies, from 2019–2026.
What is the most recent Maquet Cardiovascular, LLC recall?
Maquet Cardiovascular, LLC recalls The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI 00607567700406) is a sterile, single-use, dated Jun 2, 2026. Every Maquet Cardiovascular, LLC recall is listed on this page, newest first.
What should I do if I have a recalled Maquet Cardiovascular, LLC product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Maquet Cardiovascular, LLC recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.