International safety notice
Recall of electrode belts of the LifeVest-Systems WCD 3000 of ZOLL Lifecor Corporation
Germany / BfArM · DEU · Aug 24, 2007
Key facts
| Title | Recall of electrode belts of the LifeVest-Systems WCD 3000 of ZOLL Lifecor Corporation |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of electrode belts of the LifeVest-Systems WCD 3000 of ZOLL Lifecor Corporation |
| Manufacturer | Recall of electrode belts of the LifeVest-Systems WCD 3000 of ZOLL Lifecor Corporation |
| Models | 2007-001, 42-826-905, 3002158293-04130, 15238-3485, 15238, PROVI4, 1-412-826-9300, 15238-3495, FIE14, 412-826-9300 |
| Date | Aug 24, 2007 |
| 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