International safety notice
Recall for "Actavis-Mini-Pumpe", Actavis Deutschland GmbH & Co. KG
Germany / BfArM · DEU · May 31, 2010
Key facts
| Title | Recall for "Actavis-Mini-Pumpe", Actavis Deutschland GmbH & Co. KG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | "Actavis-Mini-Pumpe", Actavis Deutschland GmbH & Co. KG |
| Manufacturer | Recall for "Actavis-Mini-Pumpe", Actavis Deutschland GmbH & Co. KG |
| Models | 0055662, 30906359, 30926798, 02173-1674-245, 1674-0, 5391560, 2282847, 10X10, 30933530, ELOX4, 309246119, 30935114 and 13 more |
| Date | May 31, 2010 |
| 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