International safety notice
Recall for EV1000 system with software version 0.1.1.52, Edwards Lifesciences
Germany / BfArM · DEU · Apr 14, 2010
Key facts
| Title | Recall for EV1000 system with software version 0.1.1.52, Edwards Lifesciences |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | EV1000 system with software version 0.1.1.52, Edwards Lifesciences |
| Manufacturer | Recall for EV1000 system with software version 0.1.1.52, Edwards Lifesciences |
| Models | EVP01007, EV1000M, EVD01001, EVP01001, 75-305, D-85716, 145137, EVP01004, EVP00002, EVD01004, EV1000, EVD00002 and 3 more |
| Date | Apr 14, 2010 |
| 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