International safety notice
Recall for the products DERESON® (GIRO) AF, ENDES AF, ULTRADESMIT® AF and BOHRTAN® AF, esteer Pharma GmbH
Germany / BfArM · DEU · Nov 3, 2014
Key facts
| Title | Recall for the products DERESON® (GIRO) AF, ENDES AF, ULTRADESMIT® AF and BOHRTAN® AF, esteer Pharma GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the products DERESON® (GIRO) AF, ENDES AF, ULTRADESMIT® AF and BOHRTAN® AF, esteer Pharma GmbH |
| Manufacturer | Recall for the products DERESON® (GIRO) AF, ENDES AF, ULTRADESMIT® AF and BOHRTAN® AF, esteer Pharma GmbH |
| Models | 004-1001, 003-1007, 003-3013, 003-1030, 003-3002, 003-0031, 007-2011, 003-1028, 003-1017, 003-3026, 014-2020, 003-3001 and 294 more |
| Date | Nov 3, 2014 |
| 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