Home › QUICKLYPRO SRL › QP-Rehab
QP-Rehab
QUICKLYPRO SRL · Model 1.1.1 · UDI-DI 08056999860028
1
510(k) clearances
2,991
Adverse events (10 deaths)
24
Recalls
311
Facilities
Description
The QP-Rehab is a software that helps the healthcare professional, in general physiotherapist, in planning and monitoring the rehabilitation plan. The QP-Rehab allows to create a specific rehabilitation plan for each patient, to share the plan with the patient and to monitor the progress.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-03-08 | Radiometer Medical ApS | Due to potential software issue that may result in patient mix-up information. |
| 2023-02-06 | Biomerieux Inc | For users with MYLA V4.8.X / V4.9 that use VITEK MS to identify organisms as part of their workflow, AST filter rules that have been activated are not always being applied to AST r |
| 2021-09-02 | BioMerieux SA | Under certain conditions, there is a risk for a false negative result. |
| 2020-09-22 | Pentax of America Inc | There is an intermittent software issue that could affect the systems, in which an exam video for one patient (Patient A) might be copied to another patient (Patient B). This does |
| 2020-09-22 | Pentax of America Inc | There is an intermittent software issue that could affect the systems, in which an exam video for one patient (Patient A) might be copied to another patient (Patient B). This does |
| 2020-01-17 | Beckman Coulter Inc. | A security-only update was released via remote diagnostics on January 14, 2020 to customers with Windows 7 operation system. Shortly after the releases some customers reported that |
| 2019-09-25 | ENDOTRONIX | The firm have received reports of patients myCordella Hubs fully powering themselves down without interaction from the patient or Endotronix. |
| 2019-08-08 | Radiometer Medical ApS | The firm has become aware that there is a potential problem relating to the blood gas and immunoassay analyzer Systems that may result in patient mix-up when connected to some thir |
| 2019-05-20 | Opternative Inc | Lack of 510K clearance |
| 2017-12-06 | Intel-GE Care Innovations LLC | It was discovered that in certain situations, including partial sessions and when taking adhoc measurements, the patient data was not synchronizing in a timely manner with the back |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.