International safety notice
Corrective action affecting Ventak Prizm 2 DR. model 1861 manufactured by Guidant Corp.
Germany / BfArM · DEU · May 26, 2006
Key facts
| Title | Corrective action affecting Ventak Prizm 2 DR. model 1861 manufactured by Guidant Corp. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Corrective action affecting Ventak Prizm 2 DR. model 1861 manufactured |
| Manufacturer | Guidant Corp. |
| Models | 6.880, 4.366, 1.800.CARDIAC, 0641-9, 35392, 10.600, 18.000, 651.582.4000, ©2006, 11.000, 26.000, 227.3422 |
| Date | May 26, 2006 |
| 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