International safety notice
Information about iron (rust) contamination of DI Water in ADVIA® LabCell® System Tubing, Siemens Healthcare Diagnostics
Germany / BfArM · DEU · Jun 30, 2009
Key facts
| Title | Information about iron (rust) contamination of DI Water in ADVIA® LabCell® System Tubing, Siemens Healthcare Diagnostics |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Information about iron (rust) contamination of DI Water in ADVIA® LabCell® System Tubing, Siemens Healthcare Diagnostics |
| Manufacturer | Information about iron (rust) contamination of DI Water in ADVIA® LabCell® System Tubing, Siemens Healthcare Diagnostics |
| Models | ATS0003320838, ATS0002910801, 2009-05, ATS0002900750, ATS0002990808, 10591, 040D0236-01, ATS0002820747, ATS0002970806, ATS0003120819, ATS0002890750, ATS0003010813 and 7 more |
| Date | Jun 30, 2009 |
| 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