Drug recall
Panorama Patient Monitoring Network Mindray DS USA The Panorama Patient Monitoring can view recal time, store…
FDA recall event 73693 · Class II · Mindray DS USA, Inc. dba Mindray North America
Key facts
| Event ID | 73693 |
|---|---|
| Recall numbers | Z-1575-2016 |
| Recalling firm | Mindray DS USA, Inc. dba Mindray North America |
| Product type | Devices |
| Products | Panorama Patient Monitoring Network Mindray DS USA The Panorama Patient Monitoring can view recal time, store, print, graph and trend patient clinical and demographic data. The Panoram Patient… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Panorama Central Station including the work station View Station, View Station and the eGateway will revert to the year 2000 when Daylight Savings Time (DST) occurs on March 13, 2016, or under various… |
| Initiation date | Mar 9, 2016 |
| Report date | May 4, 2016 |
| Termination date | Apr 19, 2018 |
| City | Mahwah |
| State | NJ |
| Country | United States |
| FEI number | 2221819 |
At a glance
- 1–9 Products in this recall
- 10–99 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: