Devices

3.0T HD Head Neck Spine Array, Model 2415545, for GE 3.0T Excite MR System

Model / Serial
The following Serial Numbers of this device were subject to recall: 101, 102, 201, 202, 203, 204, 205, 206, 207, 309, 310.
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide, including USA, (states of CA, NJ, PA, MN, IA, MA, WI, WA, and FL) Switzerland, the United Kingdom, France, Canada and Finland.
Product Description
3.0T HD Head Neck Spine Array, Model 2415545, for GE 3.0T Excite MR System.
Manufacturer
USA Instruments Incorporated
1 Event
- Recall of 3.0T HD Head Neck Spine Array, Model 2415545, for GE 3.0T Excite MR System

Manufacturer

USA Instruments Incorporated

Manufacturer Address
USA Instruments Incorporated, 1515 Danner Dr, Aurora OH 44202-9273
Source
USFDA

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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.

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