International safety notice
Urgent Safety Notice for the Medi-Trace™ Cadence and Kendall™ Defibrillation Electrodes, Covidien
Germany / BfArM · DEU · Oct 14, 2014
Key facts
| Title | Urgent Safety Notice for the Medi-Trace™ Cadence and Kendall™ Defibrillation Electrodes, Covidien |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Medi-Trace™ Cadence and Kendall™ Defibrillation Electrodes, Covidien |
| Manufacturer | Urgent Safety Notice for the Medi-Trace™ Cadence and Kendall™ Defibrillation Electrodes, Covidien |
| Models | 40000006, 1710H, 22660R, 22660PC |
| Date | Oct 14, 2014 |
| 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