International Medical Devices Database

Manufacturer Address
GE Medical Systems LLC, 3200 N Grandview Blvd, Waukesha WI 53188-1693
Source
USFDA
2 Events
- Recall of Device Recall Definium AMX 700
- Recall of Device Recall EXCITE

2 devices in the database

Device Recall Definium AMX 700

Model / Serial
973971AMXD1, 973971AMXD2, 402449CDP1, 402449CDP2, 601426DAMX1, and 972566D700A
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Product was distributed in the following states: MS, NE, NJ, and, TX
Product Description
Definium AMX 700 Digital mobile x-ray system, GE Healthcare 3000 North Grandview Waukesha, WI

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

26 manufacturers with a similar name

Learn more about the data here

GE Medical Systems, Llc. || GE Healthcare Japan Corporation || GE Medical Systems Llc || GE Healt...

Manufacturer Parent Company (2017)
General Electric Company
Source
NIDFSINVIMA

GE Medical Systems LLC

Manufacturer Parent Company (2017)
General Electric Company
Source
NZMMDSA

GE Medical Systems LLC

Manufacturer Parent Company (2017)
General Electric Company
Source
AEMPSVFOI

GE Medical Systems LLC

Manufacturer Parent Company (2017)
General Electric Company
Manufacturer comment
Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
Source
IGJ

GE Medical Systems LLC

Manufacturer Parent Company (2017)
General Electric Company
Source
MHSIDCCCDMIS

21 more

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

Stories in your inbox

Do you work in the medical industry? Or have experience with a medical device? Our reporting is not done yet. We want to hear from you.

Tell us your story!

Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

Download the data

The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

Download all (zipped)