International safety notice
Therapy failure of the Guidant ICD Contak Renewal and Renewal
Germany / BfArM · DEU · Nov 24, 2005
Key facts
| Title | Therapy failure of the Guidant ICD Contak Renewal and Renewal |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Therapy failure of the Guidant ICD Contak Renewal and Renewal |
| Manufacturer | Therapy failure of the Guidant ICD Contak Renewal and Renewal |
| Models | INFORMA60N, H-235 |
| Date | Nov 24, 2005 |
| 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