International safety notice
Urgent Field Safety Notice for iLA activve Kits / iLA activve iLA Kit by Xenios AG
Germany / BfArM · DEU · Jul 16, 2019
Key facts
| Title | Urgent Field Safety Notice for iLA activve Kits / iLA activve iLA Kit by Xenios AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | iLA activve Kits / iLA activve iLA Kit |
| Manufacturer | Xenios AG |
| Models | 8200704, 8200643, 2019_06_EN_001.1 |
| Date | Jul 16, 2019 |
| 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