Picis Inc.: Medical Device Recall in 2013 - (Recall #: Z-1814-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

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.

Product Classification:

Class II

Date Initiated: June 21, 2013

Date Posted: August 7, 2013

Recall Number: Z-1814-2013

Event ID: 65666

Reason for Recall:

Notes associated with prescription are not printed to the prescription or to the patient chart.

Status: Terminated

Product Quantity: 35

Code Information:

Software Versions 5.2 and 5.3

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated