Maquet Cardiovascular Us Sales, Llc recalls
Every recall we track for Maquet Cardiovascular Us Sales, Llc — 32 in all, from 2018–2020 — plus the complaints and injury reports the public filed about them. 2 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Maquet Cardiovascular Us Sales, Llc peaked in 2019 (19); 32 since 2017. 6% rated “stop using now”.
All FDA recall records for Maquet Cardiovascular Us Sales, 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 | 2 | 0 | 0 | 2 |
| 2019 | 0 | 10 | 9 | 0 | 19 |
| 2020 | 2 | 5 | 4 | 0 | 11 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Maquet Cardiovascular Us Sales, 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 Us Sales, Llc recalls
15 shown- Use cautionMedical device
Maquet Cardiovascular Us Sales, Llc recalls HLS Set Advanced Model Name: BEQ-HLS 5050 USA; HLS Set Advanced 5.0, Product Code/Part Number: 70105.2797 - Product
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.
MaquetNov 20, 2020 - Use cautionMedical device
Maquet Cardiovascular Us Sales, Llc recalls Blood Monitoring Unit (BMU 40), model no. 701040852 - Product Usage: is to monitor blood parameters during
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.
MaquetSep 30, 2020 - Stop using nowMedical device
Maquet Cardiovascular Us Sales, Llc recalls Yuno Mobile Operating Table - Product Usage: Intended for support and position the patient immediately before, during
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.
MaquetSep 24, 2020 - Lower riskMedical device
Maquet Cardiovascular Us Sales, Llc recalls Maquet/Getinge Rotaflow System Console US (115 V / 60 Hz) - Product Usage: Instructions for Use - Centrifugal Pump
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.
MaquetAug 7, 2020 - Use cautionMedical device
Maquet Cardiovascular Us Sales, Llc recalls Holder HKHZ 19 for use with Quadrox-i and Quadrox-iD Neonatal / Pediatric Oxygenators, Model Number: 701047495 -
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.
MaquetJun 18, 2020 - Use cautionMedical device
Maquet Cardiovascular Us Sales, Llc recalls Avalon Elite Vascular Access Kit, Model No. 70106.3540, UDI 04037691831039
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.
MaquetFeb 20, 2020 - Use cautionMedical device
Maquet Cardiovascular Us Sales, Llc recalls Getinge 88-Series-washer disinfectors intended for cleaning, disinfection and drying Model Number: 88-5 Part Number:
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.
GetingeFeb 10, 2020 - Lower riskMedical device
Maquet Cardiovascular Us Sales, Llc recalls Getinge 46-Series Washer Disinfector Model # 46-4, Part Number:46-4-502 Product Usage: Used in facilities such as
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.
GetingeJan 16, 2020 - Lower riskMedical device
Maquet Cardiovascular Us Sales, Llc recalls Maquet Cardiopulmonary (MCP)/Getinge ROTAFLOW Drive, Model Number 701022161. The device is a component of the ROTAFLOW
Maquet recalls ROTAFLOW Drive model 701022161 due to loose ODU plug causing flow fluctuations. Affected units have specific serial numbers and UDI.
MaquetDec 3, 2019 - Lower riskMedical device
Maquet Cardiovascular Us Sales, Llc recalls Maquet Cardiopulmonary (MCP)/Getinge HLS Set Advanced 7.0. Model Number BEQ-HLS-7050 USA, Part Number 701052794
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.
MaquetJul 11, 2019 - Lower riskMedical device
Maquet Cardiovascular Us Sales, Llc recalls Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229037A Model: VST66DF
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.
MaquetMay 28, 2019 - Lower riskMedical device
Maquet Cardiovascular Us Sales, Llc recalls Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86662003 Product Usage: Usage: The Getinge 86 Series
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.
GetingeMay 20, 2019 - Use cautionMedical device
Maquet Cardiovascular Us Sales, Llc recalls GETINGE MEERA MOBILE OPERATING TABLE: (1) Part 720001B2 (2) Part 720001B0 (3) Part 720001F2 (4) Part 720001F0 (5) Part
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.
MaquetMay 6, 2019 - Use cautionMedical device
Maquet Cardiovascular Us Sales, Llc recalls Cardiohelp Emergency Drive, Part No. 70104.8002 Product Usage: The Cardiohelp Emergency Drive is used in emergencies to
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.
MaquetFeb 8, 2019 - Use cautionMedical device
Maquet Cardiovascular Us Sales, Llc recalls QUADROX-i Neonatal without integrated arterial filter and VHK 11000 (VKMO 10000-USA#QUADROX-i Neo.+Reservoir), Part
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.
MaquetOct 25, 2018
Maquet Cardiovascular Us Sales, Llc recall questions
How many recalls has Maquet Cardiovascular Us Sales, Llc had?
32 recalls from Maquet Cardiovascular Us Sales, Llc are on record with U.S. safety agencies, from 2018–2020.
What is the most recent Maquet Cardiovascular Us Sales, Llc recall?
Maquet Cardiovascular Us Sales, Llc recalls HLS Set Advanced Model Name: BEQ-HLS 5050 USA; HLS Set Advanced 5.0, Product Code/Part Number: 70105.2797 - Product, dated Nov 20, 2020. Every Maquet Cardiovascular Us Sales, Llc recall is listed on this page, newest first.
What should I do if I have a recalled Maquet Cardiovascular Us Sales, 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 Us Sales, 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.