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Devices
Device Recall EXCITE
Model / Serial
00000249264MR3, 00000257756MR7, 00000255196MR8, 00000246630MR8, 00000259107MR1, 00000248178MR6, 00000257451MR5, 00000256200MR7, 00000260871MR9, 00000252451MR0, 00000259108MR9, 00000254480MR7, 00000254482MR3, 00000256198MR3, 00000249263MR5, 00000250755MR6, 00000251090MR7, 00000GE0131001, 00000GE0213040, 00000254375MR9, 00000GE0205028, 00000GE0210034, 00000227995MR8, 00000GE0212037, 00000GE0226049, 00000GE0410083, 00000260871MR9, 00000GE0234057, 00000GE0123041, 00000GE0302068
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide, including USA, China, Finland, Germany, Israel, Italy, Korea, Spain, and Taiwan.
Product Description
GE Healthcare-Americas Signa 3.0T EXCITE Whole Body Magnetic Resonance System
Manufacturer
GE Medical Systems LLC
1 Event
Recall of Device Recall EXCITE
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Manufacturer
GE Medical Systems LLC
Manufacturer Address
GE Medical Systems LLC, 3200 N Grandview Blvd, Waukesha WI 53188-1693
Source
USFDA
Language
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