Picis ED Pulsecheck - EMR Software Application - 2125, Software Versions: 5.2 and 5.3. The application stores patient in
FDA device recall Z-1814-2013 · posted 2013-07-29 · Terminated
Recall details
- Recalling firm
- Picis Inc.
- Reason for recall
- Notes associated with prescription are not printed to the prescription or to the patient chart.
- Action taken
- Initial 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.
- Root cause
- Software change control
- Status
- Terminated
- Product code
- NSX
- Quantity affected
- 35
- Distribution
- 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.
- Date initiated
- 2013-06-21
- Date posted
- 2013-07-29
- Date terminated
- 2014-12-19
- Location
- Wakefield, MA
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