FDAFDA · Food and drugs·Recall number Z-1814-2013
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.
Published August 7, 2013 · Recall initiated: June 21, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Notes associated with prescription are not printed to the prescription or to the patient chart.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Picis Inc.
- Distributor
- 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.
- Lot
- Software Versions 5.2 and 5.3
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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