Recall Z-1814-2013— Picis Inc.
Class II · Terminated
Class II FDA medical device recall by Picis Inc., initiated 2013-06-21, terminated 2014-12-19. FDA's recall record names no specific 510(k) clearance for this event. Product: Picis ED Pulsecheck - EMR Software Application - 2125, Software Versions: 5.2 and 5.3. The application stores patient information in a database, and it may analyze and/or display the data in different formats for evaluation by healthcare professionals for informational purposes.. Reason: Notes associated with prescription are not printed to the prescription or to the patient chart..
- Recalling firm
- Picis Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2013-06-21
- Terminated
- 2014-12-19
- Firm location
- Wakefield, MA, United States
Product description
Picis ED Pulsecheck - EMR Software Application - 2125, Software Versions: 5.2 and 5.3. The application stores patient information in a database, and it may analyze and/or display the data in different formats for evaluation by healthcare professionals for informational purposes.
Reason for recall
Notes associated with prescription are not printed to the prescription or to the patient chart.
Data sourced from openFDA. This site is unofficial and independent of the FDA.