International safety notice
Batch recall for Agilia Volumat Set VL ON 70 and VL ON 72, Fresenius Kabi
Germany / BfArM · DEU · Dec 11, 2009
Key facts
| Title | Batch recall for Agilia Volumat Set VL ON 70 and VL ON 72, Fresenius Kabi |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Agilia Volumat Set VL ON 70 and VL ON 72, Fresenius Kabi |
| Manufacturer | Batch recall for Agilia Volumat Set VL ON 70 and VL ON 72, Fresenius Kabi |
| Models | 32223328, M46444600, 32122319, 484377, 32312739, 32384668, 32142679, 32413678, 32292919, 32371639, M46444100, 32413668 and 31 more |
| Date | Dec 11, 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