International safety notice
Recall for formoline L112, Certmedica
Germany / BfArM · DEU · Sep 29, 2008
Key facts
| Title | Recall for formoline L112, Certmedica |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | formoline L112, Certmedica |
| Manufacturer | Recall for formoline L112, Certmedica |
| Models | A80601.3, A80604, A80606, A80508.5, 2011-12, A80610, A80609, A80605, A80505, A80602, 2011-1, A80507 and 1 more |
| Date | Sep 29, 2008 |
| 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