Medical Device Recalls
-
1 to 6 of 6 Results
510(K) Number: K103327 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scann... | 2 | 10/20/2020 | GE Healthcare, LLC |
GE Healthcare, Discovery MR750w | 2 | 07/06/2016 | GE Healthcare, LLC |
GE Healthcare Discovery MR450, Discovery MR750, Optima MR450w, Optima MR450w equipped with the GEM o... | 2 | 05/01/2014 | GE Healthcare, LLC |
GE Healthcare, Discovery MR450, Discovery MR750, Optima MR450w, Optima MR 450w GEM, Discovery MR750w... | 2 | 04/21/2014 | GE Healthcare, LLC |
GE 1.5T Signa HDxt, 3.0T Signa HDxt, Signa Vibrant, HD23 Software and the following model numbers: 2... | 2 | 09/23/2013 | GE Healthcare, LLC |
GE Healthcare, Discovery MR750w 3.0T System. Part Number: 5352293. Product Usage: It is indica... | 2 | 04/11/2013 | GE Healthcare, LLC |
-