International safety notice
Recall for Ambix activ ambulatory Set and Ambix activ stationary Set, Fresenius Kabi
Germany / BfArM · DEU · Sep 11, 2009
Key facts
| Title | Recall for Ambix activ ambulatory Set and Ambix activ stationary Set, Fresenius Kabi |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Ambix activ ambulatory Set and Ambix activ stationary Set, Fresenius Kabi |
| Manufacturer | Recall for Ambix activ ambulatory Set and Ambix activ stationary Set, Fresenius Kabi |
| Models | 2892098, 32083349, E4302, 32053738, E4529, 2892095, 421327, 32231968, 32104778, 32116718, 32075639, 32225628 and 5 more |
| Date | Sep 11, 2009 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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