Panorama Patient Monitoring Network — Class II medical device recall Z-1675-2015
Terminated recall by Mindray DS USA, Inc. dba Mindray North America, reported 2015-06-03, distributed nationwide. Software anomaly in the Panorama System software version 8.9 that manifests when the Panorama is in use with M
| Recall number | Z-1675-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mindray DS USA, Inc. dba Mindray North America, Mahwah, NJ, United States |
| Recall initiated | 2015-03-12 |
| Classified | 2015-05-26 |
| Reported by FDA | 2015-06-03 |
| Terminated | 2017-03-28 |
| Distributed | Nationwide (US) |
| Quantity | 4 units |
| Reason classes | software |
| Model numbers | 0998-00-0708-01 |
Product
Panorama Patient Monitoring Network, Multi- Parameter Patient Monitor (with Arrhythmia Detection and Alarm. Part number 0998-00-0708-01. The Panorama Network includes the Panorama Telemetry System, which acquires and monitors physiological data for ambulating patients within a defined coverage area.
Reason for recall
Software anomaly in the Panorama System software version 8.9 that manifests when the Panorama is in use with Mindray Passport V Monitor. Arrhythmia alarms which were previously displayed on both the Passport V and Panorama will not be displayed on the Panorama following a restart of either system (due to communication loss, restart, etc.).
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-1675-2015. 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.