Every recall we track for Maquet Cardiovascular, LLC — 246 in all — plus the complaints and injury reports the public filed about them.
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 recalls Heartstring III Proximal Seal System (4.3 MM) due to risk of hemostasis failure during vascular surgery. Affected units include specific serial numbers and model HSK-3043. Consumers should contact Maquet for details.
Maquet recalls Heartstring III Proximal Seal System (3.8 MM) due to risk of hemostasis failure during vascular surgery. Affected units have specific serial numbers and model numbers.
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.
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 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.
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.
Maquet recalls Vasoview Hemopro 2 (VH-4001) endoscopic vessel harvesting systems due to potential heater wire detachment or silicone peeling from jaws, which could cause injury during surgery.
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.
Maquet recalls Acrobat-i Positioner (model C-XP-5000Z) due to potential sterility compromise in 2-year shelf life. Affected units have specific batch numbers; consumers should check if they own the product.
Maquet recalls Acrobat SUV Vacuum Stabilizer System (model C-OM-9000Z) due to potential sterility compromise in its 2-year shelf life. Affected units have specific batch numbers.
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.
Maquet recalls VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System due to C-Ring wire straightening causing improper device positioning. 27 complaints reported between March 22 and April 30, 2024.
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.
Maquet recalls VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems with potential fluid ingress into the handle causing improper cautery function. Affected models include VH-3500 and VH-3000-W.
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.
Maquet recalls certain express chest drains due to risk of infection if not kept upright. Patients may face infection, abscess, sepsis, or death if device is not positioned correctly.
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.
Maquet recalls Vasoview Hemopro VH-3500 endoscopic vessel harvesting system due to potential polyimide particles entering arterial grafts during coronary or peripheral bypass surgery.
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 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.
Maquet recalls Vasoview 6 Pro (VV6) endoscopic vessel harvesting system with incorrect box artwork that could lead to confusion about the device model.
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.
Maquet recalls ACROBAT V Vacuum Off-Pump System (Part C-OM-9100S) due to risk of unstable chest stabilization during surgery, potentially causing device release or procedural delays.
Maquet recalls ACROBAT-i Vacuum Stabilizer System (Part C-OM-10000) due to potential stabilization failure during cardiac surgery, risking device displacement or procedural delays.
Maquet recalls ACCESSRAIL Standard Blade (SB-1000) and Deep Blades (C-DB-1000) for potential instability during cardiac surgery, risking device release or procedural delays.
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.
Maquet recalls VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System (Model C-VH-350: Lot 3000280189, 3000276183) due to unsterilized batches. Affected users should contact Maquet for details.
Maquet recalls VASOVIEW HEMOPRO endoscopic vessel harvesting system (model C-VH-3000-W) due to unsterilized batches. Affected units may cause infection if used in surgery.
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.
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.
Maquet recalls Hemopro 2 with Vasoshield Model VH-4001 due to potential ink chip causing patient harm. Affected units have specific serial numbers.
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.
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.
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.
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.
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.
Maquet recalls Hemashield Gold Knitted Microvel Double Velour Vascular Grafts with potential small holes at seam lines causing intra-operative bleeding. Product code M002020955010, serial numbers listed.
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. Contact for remedy.
Maquet recalls Hemashield Platinum Woven Double Velour Vascular Grafts with potential small holes at seam lines causing intra-operative bleeding. Affected units have specific serial numbers.
Maquet recalls Hemashield Platinum Woven Double Velour Vascular Grafts with potential small holes at seam lines causing intra-operative bleeding. Affected units have specific serial numbers.
Maquet recalls Hemashield Platinum Vascular Grafts with potential small holes at seam lines causing intra-operative bleeding. Affected units have specific serial numbers. Contact for remedy.
Maquet recalls Hemashield Platinum Woven Double Velour Vascular Grafts with potential small holes at seam lines causing intra-operative bleeding. Affected units have specific serial numbers.
Maquet recalls Hemashield Platinum Woven Double Velour Vascular Grafts with potential small holes at seam lines causing intra-operative bleeding during surgery.
Maquet recalls Hemashield Platinum woven vascular grafts with potential small holes at seam lines causing intra-operative bleeding. Affected units have specific serial numbers.
Maquet recalls Hemashield Gold Knitted Microvel Double Velour Vascular Grafts with potential small holes at seam lines causing intra-operative bleeding. Affected product codes and serial numbers listed.
Maquet recalls Hemashield Platinum Woven Double Velour Vascular Grafts with potential small holes at seam lines causing intra-operative bleeding. Affected product codes and serial numbers listed.
Maquet recalls Hemashield Platinum Woven Double Velour Vascular Grafts with potential small holes at seam lines causing intra-operative bleeding. Product code M00202175828P0, serial numbers listed. Contact for remedy.
Maquet recalls Hemashield Platinum Woven Double Velour Vascular Grafts with potential small holes at seam lines causing intra-operative bleeding. Affected units have specific serial numbers.
Maquet recalls Hemashield Platinum Woven Double Velour Vascular Grafts with potential small holes at seam lines causing intra-operative bleeding. Affected units have specific serial numbers.
Maquet recalls Hemashield Platinum Woven Double Velour Vascular Grafts (Product Code M00202175428T0) due to potential small holes at seam lines causing intra-operative bleeding. Affected units have specific serial numbers.
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.
Maquet recalls Hemashield Platinum Woven Double Velour Vascular Grafts with potential small holes at seam lines causing intra-operative bleeding. Affected units have specific serial numbers.
Maquet recalls Hemashield Platinum Woven Double Velour Vascular Grafts with potential small holes at seam lines causing intra-operative bleeding. Affected units have specific serial numbers.
Maquet recalls Hemashield Platinum Woven Double Velour Vascular Grafts with potential small holes at seam lines causing intra-operative bleeding. Affected units have specific serial numbers.
Maquet recalls Hemashield Platinum Woven Double Velour Vascular Grafts due to potential small holes at seam lines causing intra-operative bleeding. Affected units have specific serial numbers.
Maquet recalls Hemashield Gold Knitted Microvel Double Velour Vascular Grafts with potential small holes at seam lines causing intra-operative bleeding. Product code M002020955890, serial numbers 1176626841, 117662481: check your grafts for seam line holes.
Maquet recalls Hemashield Platinum Woven Double Velour Vascular Grafts with potential small holes at seam lines causing intra-operative bleeding. Affected units have specific serial numbers.
Maquet recalls Hemashield Platinum Woven Double Velour Vascular Grafts with potential small holes at seam lines causing intra-operative bleeding. Affected units have specific serial numbers.
