International safety notice
Corrective action for the CA 19-9 Test, Siemens Healthcare
Germany / BfArM · DEU · Dec 9, 2011
Key facts
| Title | Corrective action for the CA 19-9 Test, Siemens Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the CA 19-9 Test, Siemens Healthcare |
| Manufacturer | Corrective action for the CA 19-9 Test, Siemens Healthcare |
| Models | 19882, 35.2–52.8, 19863, 54532, 19883, 54533, 13.4–27.8, 19911, 19893, 078D1144-01, 19862, 19881 and 29 more |
| Date | Dec 9, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers 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