International safety notice
Recall of HeartStart FR2+ Automated External Defibrillators, models M3860A, M3861A, M3840A and M3841A from Philips Medizin Systeme Böblingen
Germany / BfArM · DEU · Jan 26, 2007
Key facts
| Title | Recall of HeartStart FR2+ Automated External Defibrillators, models M3860A, M3861A, M3840A and M3841A from Philips Medizin Systeme Böblingen |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of HeartStart FR2+ Automated External Defibrillators, models M3860A, M3861A, M3840A and M3841A from Philips Medizin Systeme Böblingen |
| Manufacturer | Recall of HeartStart FR2+ Automated External Defibrillators, models M3860A, M3861A, M3840A and M3841A from Philips Medizin Systeme Böblingen |
| Models | M3841A, 1-800-264-3342, 1-800-263-3342, M3861A, M3860A, M3840A, 98121-1825 |
| Date | Jan 26, 2007 |
| 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