International safety notice
Guidant recalls the implantable pacemaker models Pulsar, Pulsar Max, Pusar Max II, Discovery, Discovery II, Meridian,Virtus Plus II, Intelis II and Contak TR
Germany / BfArM · DEU · Feb 16, 2006
Key facts
| Title | Guidant recalls the implantable pacemaker models Pulsar, Pulsar Max, Pusar Max II, Discovery, Discovery II, Meridian,Virtus Plus II, Intelis II and Contak TR |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Guidant recalls the implantable pacemaker models Pulsar, Pulsar Max, Pusar Max II, Discovery, Discovery II, Meridian,Virtus Plus II, Intelis II and Contak TR |
| Manufacturer | Guidant recalls the implantable pacemaker models Pulsar, Pulsar Max, Pusar Max II, Discovery, Discovery II, Meridian,Virtus Plus II, Intelis II and Contak TR |
| Models | B4TILE, 92221-0, 922210, 35392, 781000, W71ILE, 16.000, EVNLUA60N, 1186T, 2.500, 92221-606, 14831 and 2 more |
| Date | Feb 16, 2006 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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