Reported Aug 7, 2013 · Terminated
Picis ED Pulsecheck - EMR Software Application - 2125, Software Versions: 5.2 and 5.3. The application stores patient…
Picis Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Picis Inc. · 100 Quannapowitt Parkway · Wakefield, MA · 01880
Is this the product you have?
- Picis ED Pulsecheck - EMR Software Application - 2125
- Software Versions5.2 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
- Lot codes and dates
- Software Versions 5.2 and 5.3
- Amount recalled
- 35
Where it was sold
Why it was recalled
Notes associated with prescription are not printed to the prescription or to the patient chart.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Picis Inc. recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.