Medical Device Recalls
-
1 to 7 of 7 Results
510(K) Number: K081496 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Discovery PET/CT 610 Product Usage: The systems are intended for head and whole body attenuation... | 2 | 06/19/2019 | GE Healthcare, LLC |
Optima PET/CT 560, 560FX Product Usage: The systems are intended for head and whole body attenua... | 2 | 06/19/2019 | GE Healthcare, LLC |
GE Healthcare Discovery PET/CT 600,610, 690, 710: Optima PET/CT 560. 560FX X-ray system | 2 | 06/12/2017 | GE Healthcare, LLC |
LightSpeed 16 (MDAS only , , 2339985 LightSpeed 4.0 CT Scanner System - The LightSpeed 4.0 CT Scan... | 2 | 03/04/2016 | GE Medical Systems, LLC |
GE Healthcare, PET Discovery 610, Discovery 710, Discovery 600 and Discovery 690. The GE Discover... | 2 | 02/14/2014 | GE Healthcare, LLC |
GE PET Discovery 610, PET Discovery 710. Intended for head and whole body attenuation corrected P... | 2 | 10/17/2013 | GE Healthcare, LLC |
GE, VCT for Discovery VCT, Discovery RX VCT, and Discovery PET/CT 690, Lightspeed VCT, Discovery CT7... | 2 | 04/29/2013 | GE Healthcare, LLC |
-