International safety notice
Corrective action of the samaritan PAD 500P public access defibrillators, HeartSine Technologies
Germany / BfArM · DEU · Mar 24, 2014
Key facts
| Title | Corrective action of the samaritan PAD 500P public access defibrillators, HeartSine Technologies |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Corrective action of the samaritan PAD 500P public access defibrillators, HeartSine Technologies |
| Manufacturer | Corrective action of the samaritan PAD 500P public access defibrillators, HeartSine Technologies |
| Models | 99.04, 93.01, 96.97, 13341, 96.72, 91.36, 96.05, 97.95, 99.91, 286056, 99.01, 500PDATA and 3 more |
| Date | Mar 24, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 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