International safety notice
Safety Notice concerning a corrective action of the Magnetic Resonance Imaging System MSK 1.5T Extreme, GE Healthcare
Germany / BfArM · DEU · Aug 30, 2011
Key facts
| Title | Safety Notice concerning a corrective action of the Magnetic Resonance Imaging System MSK 1.5T Extreme, GE Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Safety Notice concerning a corrective action of the Magnetic Resonance Imaging System MSK 1.5T Extreme, GE Healthcare |
| Manufacturer | Safety Notice concerning a corrective action of the Magnetic Resonance Imaging System MSK 1.5T Extreme, GE Healthcare |
| Models | 9900INNOVATIONDRIVE, GEHEALTHCAREHASRECENTLYBECOMEAWARETHATANEXPOSEDHIGHVOLTAGEGRADIENTWIREINTERNALTOTHEMSK1.5TEXTREME, WI53226, 165VDC, FMI60810, BETWEEN“06012008001”TO“12222010, MSK1.5TEXTREME, 20110818, ONTHEMSK1.5TEXTREME, 001”.THESYSTEMIDENTIFICATIONNUMBERISLOCATEDONTHEREARCOVEROFTHEMAGNET, FMI60810_FSN_ENGLISH |
| Date | Aug 30, 2011 |
| 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