Panaroma Central Station Product Usage: This device can view real time — Class II medical device recall Z-1156-2014
Terminated recall by Mindray DS USA, Inc. dba Mindray North America, reported 2014-03-19, distributed nationwide. Mindray has identified two issues with the Panorama Central Station. Full Disclosure data may lag behind the P
| Recall number | Z-1156-2014 |
|---|---|
| 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 | 2014-01-08 |
| Classified | 2014-03-07 |
| Reported by FDA | 2014-03-19 |
| Terminated | 2015-01-21 |
| Distributed | Nationwide (US) |
| Quantity | 732 units |
Product
Panaroma Central Station Product Usage: This device can view real time, store, print, graph, and trend patient clinical and demographic data. The device can also set independent alarm limits for data send by the bedside monitor.
Reason for recall
Mindray has identified two issues with the Panorama Central Station. Full Disclosure data may lag behind the Panorama system time clock when the Panorama Central Station is in use with Mindray¿s V-Series Monitor. Additionally, event indicators lag behind the Panorama system time clock when the Panorama Central Station is in use with a Panorama Telepack.
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-1156-2014. 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.