Philips Visicu
Philips Visicu appears in FDA public data with 2 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1708-2017, Class II) was initiated on March 2, 2017.
Summary
- Total Recalls
- 2
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-1708-2017 | Class II | eCare Coordinator Product Usage: is software intended for use in data aggregation, patient inte | March 2, 2017 |
| Z-1557-2016 | Class II | eCareCoordinator allows the customer to schedule patient tasks (i.e., take weight measurement, take | March 10, 2016 |