Home / Brands / Philips Visicu
Philips Visicu Recalls
2 recalls on record · May 4, 2016 to April 12, 2017 · Medical Devices
Recalls by year
16
17
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
April 12, 2017Medical DevicesFDA
Philips Visicu recalls eCare Coordinator Product Usage: is software intended for use in data aggregation, patient interaction facilitation
Hazard: eCareCoordinator (eCC) is intended for use in data aggregation, patient interaction facilitation, storage and clinical information management with independent physiological devices and ancillary systems that are connected either directly or through networks. The software is intended to provide patient information from the patient location through networking technology to a remote care team. A software defect was discovered in the Philips eCareCoordinator (eCC) Clinical User Interface that can at times cause missing or redundant data to be saved without notification to the user.
May 4, 2016Medical DevicesFDA
Philips Visicu recalls eCareCoordinator allows the customer to schedule patient tasks (i.e., take weight measurement, take blood pressure).
Hazard: The adherence check generates a software error. Two issues occur as a result of the software error: 1) No adherence flag is generated for that day; 2) No task is generated for the date 14 days later. An error message is generated and forwarded to operations. Subsequently, for days in which no task was generated, patient will not get a reminder on the tablet to take a measurement. If the pa