Picis ED Pulsecheck — Class II medical device recall Z-1814-2013
Terminated recall by Picis Inc., reported 2013-08-07, distributed nationwide. Notes associated with prescription are not printed to the prescription or to the patient chart.
| Recall number | Z-1814-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Picis Inc., Wakefield, MA, United States |
| Recall initiated | 2013-06-21 |
| Classified | 2013-07-29 |
| Reported by FDA | 2013-08-07 |
| Terminated | 2014-12-19 |
| Distributed | Nationwide (US) |
| Quantity | 35 |
Product
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.
Reason for recall
Notes associated with prescription are not printed to the prescription or to the patient chart.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1814-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.