International safety notice
Corrective action and recall for Rotem coagulation analyzers of Pentapharm
Germany / BfArM · DEU · Oct 11, 2006
Key facts
| Title | Corrective action and recall for Rotem coagulation analyzers of Pentapharm |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Rotem coagulation analyzers of Pentapharm |
| Manufacturer | Corrective action and recall for Rotem coagulation analyzers of Pentapharm |
| Models | 1-866-342-0011, 78758, M1710, E1505, 2006-08-17, 20060817 |
| Date | Oct 11, 2006 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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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