Health Harmony Mobile application software Product Usage: Care Innovations Health Harmony Mobile is intended as a communication tool to display medical device data from third party devices for patients to view, and to collect assessment (question & answers) from patients in the home.Care Innovations Health Harmony Mobile is intended as a communication tool to display medical device data from third party devices for patients to view, and to collect assessment (question & answers) from patients in the home. Patients can review their stored vital sign measurements (captured outside of Health Harmony Mobile) and receive educational and motivational content from caregivers.
FDA Recall Z-2442-2018 · Posted None
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Recalling FirmIntel-GE Care Innovations LLC
Recall StatusTerminated
Product CodeOUG
Date Initiated2017-12-06
Date Terminated2020-10-23
Product Quantity1302
Reason for Recall
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 backend database, resulting in the patient's clinician not getting patient data tor one or two days.
Firm Action
The firm sent e-mails to their 4 consignees during the first week of December 2017. with the following information:
As you may know, we have discovered a technical issue in our Health Harmony product that may result in some patient data not being transmitted to the Maestro 2 clinical dashboard in a timely manner (i.e. vital signs, health session
answers). This can also manifest as a patient unable to execute their health session. Our investigation shows that in some cases, your clinical team may not receive patient readings in the normal timeframe. We take this issue very seriously. We are focused on investigating the root cause while also mitigating the effects on patient management as our engineering team solves the
issue.
While we continue to investigate this issue, we are developing a mitigation and will begin deploying shortly. This includes a progress notice and a message on the patient tablet when the system is synchronizing and transmitting
results. The message will remind patients to stay in the program until their results have successfully uploaded and transmitted.
Please be assured we are urgently working on addressing this issue.
Your Care Innovations program management team will follow up with you to discuss potential impact on your standard of care, the next steps and answer any questions you may have about this situation.
Thank you for your continued patience,
Marcus Grindstaff
CHIEF OPERATING OFFICER
Care Innovations
Cell: 916.548.3013
Root Cause
Under Investigation by firm
Distribution Pattern
US Nationwide Distribution in the states of CO, ID, PA, and LA
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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