Drug recall
Picis ED Pulsecheck - EMR Software Application - 2125, Software Versions: 5.2 and 5.3. The application stores…
FDA recall event 65666 · Class II · Picis Inc.
Key facts
| Event ID | 65666 |
|---|---|
| Recall numbers | Z-1814-2013 |
| Recalling firm | Picis Inc. |
| Product type | Devices |
| Products | 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Notes associated with prescription are not printed to the prescription or to the patient chart. |
| Initiation date | Jun 21, 2013 |
| Report date | Aug 7, 2013 |
| Termination date | Dec 19, 2014 |
| City | Wakefield |
| State | MA |
| Country | United States |
| FEI number | 3005244943 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: