International safety notice
Corrective action for Avantx-E, Innova 2000, 2100IQ, 3100/3100IQ, 4100/4100IQ and 2121IQ/3131IQ, GE Healthcare
Germany / BfArM · DEU · Jul 4, 2008
Key facts
| Title | Corrective action for Avantx-E, Innova 2000, 2100IQ, 3100/3100IQ, 4100/4100IQ and 2121IQ/3131IQ, GE Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Avantx-E, Innova 2000, 2100IQ, 3100/3100IQ, 4100/4100IQ and 2121IQ/3131IQ, GE Healthcare |
| Manufacturer | Corrective action for Avantx-E, Innova 2000, 2100IQ, 3100/3100IQ, 4100/4100IQ and 2121IQ/3131IQ, GE Healthcare |
| Models | 21000, 13004, RP2138, 31000, 1-80043B, 41000, 53226 |
| Date | Jul 4, 2008 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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