International safety notice
Recall of Pentapharm extended for reagents ex-TEM
Germany / BfArM · DEU · Jan 12, 2009
Key facts
| Title | Recall of Pentapharm extended for reagents ex-TEM |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | reagents ex-TEM |
| Manufacturer | Recall of Pentapharm extended for reagents ex-TEM |
| Models | DE-81829, 2008-09-27, 2008-11, DE209487304, 0209487304, 41267801, 132082, 13485, 503-03 |
| Date | Jan 12, 2009 |
| 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