International safety notice
Urgent Safety Notice for certain models of implantable left ventricular LV CRT bipolar leads QuickSite und QuickFlex, St. Jude Medical
Germany / BfArM · DEU · May 24, 2012
Key facts
| Title | Urgent Safety Notice for certain models of implantable left ventricular LV CRT bipolar leads QuickSite und QuickFlex, St. Jude Medical |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | certain models of implantable left ventricular LV CRT bipolar leads QuickSite und QuickFlex, St. Jude Medical |
| Manufacturer | Urgent Safety Notice for certain models of implantable left ventricular LV CRT bipolar leads QuickSite und QuickFlex, St. Jude Medical |
| Models | 1156T, 0.019, 0.047, 1058T, 91342-3577, 0.042, 0.033, 0.063, 0.028, 0.043, 1258T, 1158T and 12 more |
| Date | May 24, 2012 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers in FDA data
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