International safety notice
Recall of the PadPro Adult Radiotranslucent defibrillation electrodes 2516Z and 2516M from ConMed
Germany / BfArM · DEU · Apr 13, 2007
Key facts
| Title | Recall of the PadPro Adult Radiotranslucent defibrillation electrodes 2516Z and 2516M from ConMed |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the PadPro Adult Radiotranslucent defibrillation electrodes 2516Z and 2516M from ConMed |
| Manufacturer | Recall of the PadPro Adult Radiotranslucent defibrillation electrodes 2516Z and 2516M from ConMed |
| Models | YOIOS06LLO, 2316M, 13602, 2516Z, 2316Z, 1.1605-3, Y092805, Y052605-4, 40605-1, 2516M—, 2S16Z, 315-6243089 and 5 more |
| Date | Apr 13, 2007 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 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