International safety notice
Field Safety Notice concerning X-ray systems Innova 2100IQ, 3100, 3100IQ, 4100, 4100IQ, 2121IQ and 3131IQ with tube chiller manufactured between 08/01/08 and 04/01/09, GE Healthcare
Germany / BfArM · DEU · Jun 16, 2009
Key facts
| Title | Field Safety Notice concerning X-ray systems Innova 2100IQ, 3100, 3100IQ, 4100, 4100IQ, 2121IQ and 3131IQ with tube chiller manufactured between 08/01/08 and 04/01/09, GE Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Field Safety Notice concerning X-ray systems Innova 2100IQ, 3100, 3100IQ, 4100, 4100IQ, 2121IQ and 3131IQ with tube chiller manufactured between 08/01/08 and 04/01/09, GE Healthcare |
| Manufacturer | Field Safety Notice concerning X-ray systems Innova 2100IQ, 3100, 3100IQ, 4100, 4100IQ, 2121IQ and 3131IQ with tube chiller manufactured between 08/01/08 and 04/01/09, GE Healthcare |
| Models | 310010, 21001, RP2138, 4100Q, 313110, 1-800-4371171, 41001Q, 31001Q, 21000, 53226 |
| Date | Jun 16, 2009 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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