International safety notice
Recall of the ambIT Intermittent Ambulatory Infusion Pump from Sorenson
Germany / BfArM · DEU · Jun 28, 2006
Key facts
| Title | Recall of the ambIT Intermittent Ambulatory Infusion Pump from Sorenson |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the ambIT Intermittent Ambulatory Infusion Pump from Sorenson |
| Manufacturer | Recall of the ambIT Intermittent Ambulatory Infusion Pump from Sorenson |
| Date | Jun 28, 2006 |
| 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