ClearanceBrief
Recall Z-1814-2013 ยท NSX

Picis Inc.

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.

DateJul 29, 2013 (initiated Jun 21, 2013)
StatusTerminated
ReasonNotes associated with prescription are not printed to the prescription or to the patient chart.
Root causeSoftware change control
ActionInitial customer notifications were sent via email on June 21, 2013 informing consignees of the recall and providing further instruction regarding the software solution. Consignees were provided with recommended actions until they receive the necessary update.
Quantity35
DistributionNationwide Distribution, including the states of: AK, AR, AZ, CA, CO, DC, DE, FL, GA, ID, IN, MA, MD, MO, NH, NJ, OH, OR, SC, TN, WA, and WV.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.