International safety notice
Safety Notice / Corrective action for the Dimension Vista® 500 and Dimension Vista® 1500 systems, Siemens Healthcare Diagnostics
Germany / BfArM · DEU · May 3, 2014
Key facts
| Title | Safety Notice / Corrective action for the Dimension Vista® 500 and Dimension Vista® 1500 systems, Siemens Healthcare Diagnostics |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Dimension Vista® 500 and Dimension Vista® 1500 systems, Siemens Healthcare Diagnostics |
| Manufacturer | Safety Notice / Corrective action for the Dimension Vista® 500 and Dimension Vista® 1500 systems, Siemens Healthcare Diagnostics |
| Models | 10444801, 10706557, 14-19, 10444802, 10284473, 10488224, 19714-6101 |
| Date | May 3, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1