Every recall we track for Maquet Cardiovascular Us Sales, Llc — 32 in all — plus the complaints and injury reports the public filed about them.
Maquet recalls HLS Set Advanced 7.0 devices (model BEQ-HLS 7050) due to sterility barrier breaches. These devices are used for cardiac support. Affected units include specific lot codes.
Maquet recalls HLS Set Advanced 5.0 models with product code 70105.2797 due to sterility barrier breaches that could cause infections during cardiac surgery.
Maquet recalls BMU 40 blood monitoring units with model 701040852 due to insufficient PCB creepage distance (1.8mm vs required 4mm), potentially causing electrical issues during cardiac surgery.
Maquet recalls Yuno II Mobile Operating Tables with serial numbers SN 1-SN 13 (US) and SN 1-SN 62 (OUS) due to risk of electric shock from exposed wiring. Affected units must be stopped immediately.
Maquet recalls Yuno Mobile Operating Tables with exposed electrical components that could cause electric shock. Affected units have specific serial numbers; stop using immediately to prevent injury.
Maquet recalls US Rotaflow System Consoles with serial numbers 94175452-94175518 due to incorrect serial number in instructions. This may cause confusion in device use.
Maquet recalls Holder HKHZ 19 for use with Quadrox-i and Quadrox-iD neonatal/pediatric oxygenators due to potential failure to securely hold oxygenators during use. Affected units have lot number 70128207.
Maquet recalls Avalon Elite Vascular Access Kit model 70106.3540 due to incorrect arterial needle included in some kits. Affected kits may cause injury if used improperly.
Getinge 88-Series washer disinfectors with model 88-5 may leak due to ruptured spot welds, risking slips or infection. Affected units have specific serial numbers. Contact manufacturer for details.
Getinge 46-Series Washer Disinfector Model 46-4 with missing deionized water intake may not install properly. No serious injuries reported. Affected units have specific serial numbers.
Getinge 46-Series Washer Disinfector Model 46-4 (serials WAA090630 etc.) may not be properly installed due to missing deionized water intake. No serious injuries reported.
Maquet recalls ROTAFLOW Drive model 701022161 due to loose ODU plug causing flow fluctuations. Affected units have specific serial numbers and UDI.
Maquet recalls specific cardiopulmonary sets due to reversed connectors causing improper priming and potential device malfunction. Affected units have model BEQ-HLS-7050 and part number 701052794.
Maquet recalls VOLISTA StandOP Surgical Lights (model VST60DF) due to potential coating cracks that could cause particles to fall into the surgical field, risking patient infection. Affected units have specific serial numbers.
Maquet recalls VOLISTA StandOP Surgical Lights with serial numbers 31000-38027 due to potential light head coating cracks that could cause surgical field contamination and patient infection.
Maquet recalls VOLISTA StandOP Surgical Lights with potential cracked light head forks that could drop particles into surgical fields, risking patient infection. Affected units have specific serial numbers.
Maquet recalls VOLISTA StandOP Surgical Lights (model VST60SF) due to potential light head coating cracks that could cause surgical field infections. Affected units have specific serial numbers.
Maquet recalls VOLISTA StandOP Surgical Lights with potential for cracked light heads that could cause surgical infections. Affected models include VLT600SF STP with specific serial numbers. Contact for repair or replacement.
Maquet recalls VOLISTA StandOP Surgical Lights with model VLT600SF AIM STP due to potential cracking of light head forks that could cause surgical site infections. Affected units have specific serial numbers.
Maquet recalls VOLISTA StandOP Surgical Lights with potential for cracked light heads to fall into surgical fields, risking patient infection. Affected units include specific model and serial numbers.
Maquet recalls VOLISTA StandOP Surgical Lights with serial numbers 25004-38028 due to potential cracking of light head forks that could cause surgical site infections.
Maquet recalls VOLISTA StandOP Surgical Lights with potential cracked light head forks that could cause surgical infections. Affected units have specific model and serial numbers.
Maquet recalls VOLISTA StandOP Surgical Lights with potential for cracked light heads that could cause surgical infections. Affected models include VLT400SF STP with specific serial numbers.
Maquet recalls VOLISTA StandOP Surgical Lights with potential for cracked light heads that could drop particles into surgical fields, risking patient infection. Affected units include specific model and serial numbers.
Maquet recalls VOLISTA StandOP Surgical Lights with potential for cracked light heads to fall into surgical fields, risking patient infection. Affected units include specific model and serial numbers.
Maquet recalls VOLISTA StandOP Surgical Lights with model VST66DF and specific serial numbers due to risk of cracked light head forks causing surgical site infections. Affected units include serial numbers 500040-500050, 500069.
Getinge 86-Series medical washer-disinfectors with specific serial numbers may have inlet pump hose that collapses during use, risking improper cleaning. Affected units must be checked and repaired.
Getinge 86-Series medical washer-disinfectors with part number S-86662003 may have inlet pump hose that collapses during use, causing poor cleaning. Affected units include specific serial numbers.
Maquet recalls Meera Mobile Operating Tables with specific serial numbers due to risk of electric shock from exposed components. Affected models include Part 720001B2, B0, F2, F0, and 710001B2/B0/F0.
Maquet recalls specific Cardiohelp Emergency Drive models due to potential incorrect reassembly during servicing, which may cause inadequate operation in emergencies. Affected serial numbers listed.
Maquet recalls QUADROX-i Neonatal devices with specific part numbers due to potential blood leakage when using a reducing screw adapter, risking clinically relevant blood loss during patient connection.
Maquet recalls Quadrox-i Neonatal without integrated arterial filter and VHK 11000 units with potential blood leakage at blood inlet connector using reducing screw adapter 1/4 x 3/16.
