Home / Recalls / Medical Devices
Picis Inc. recalls Picis ED Pulsecheck - EMR Software Application - 2125, Software Versions: 5.2 and 5.3. The application stores patient i
Recalled August 7, 2013 · FDA recall Z-1814-2013 · Picis
Hazard
Notes associated with prescription are not printed to the prescription or to the patient chart. · FDA Class II
Units
35
Sold at
Nationwide 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.
Description
Notes associated with prescription are not printed to the prescription or to the patient chart.
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.
Manufacturer(s)
Picis Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →