International safety notice
Corrective Action of Siemens Healthcare Diagnostics Inc. for Dimension Vista System V-LYTE Integrated Multisensor
Germany / BfArM · DEU · Nov 12, 2008
Key facts
| Title | Corrective Action of Siemens Healthcare Diagnostics Inc. for Dimension Vista System V-LYTE Integrated Multisensor |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Dimension Vista System V-LYTE Integrated Multisensor |
| Manufacturer | Corrective Action of Siemens Healthcare Diagnostics Inc. for Dimension Vista System V-LYTE Integrated Multisensor |
| Models | 19714-6101, 800-441-9250 |
| Date | Nov 12, 2008 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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