International safety notice
Corrective action for Dimension Vista® Myoglobin Calibrator (MYO CAL), Siemens Healthcare Diagnostics Inc.
Germany / BfArM · DEU · Dec 16, 2014
Key facts
| Title | Corrective action for Dimension Vista® Myoglobin Calibrator (MYO CAL), Siemens Healthcare Diagnostics Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Dimension Vista® Myoglobin Calibrator (MYO CAL), Siemens Healthcare Diagnostics Inc. |
| Manufacturer | Corrective action for Dimension Vista® Myoglobin Calibrator (MYO CAL), Siemens Healthcare Diagnostics Inc. |
| Models | 4FD085, GPF-003, 10445191, GP-003, 2013-12-31, 19714-6101, 14-88, KC624 |
| Date | Dec 16, 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