Skip to main content
All Recalls

Every Neurologica Corporation Recall

Sorted by most recent. Click any recall for full details.

8 recalls
High RiskFDA
Neurologica Corporation
Samsung Digital Diagnostic Mobile X-ray System, Model GM85.
Diagnostic Devices·261 affected·Dec 28, 2023
High RiskFDA
Neurologica Corporation
OmniTom/OmniTom Elite- X-ray computed tomography applications for anatomy that can be imaged in the 40 cm aperture, primarily head and ne...
Medical Devices·48 affected·Jun 6, 2023
High RiskFDA
Neurologica Corporation
OmniTom Computed tomography x-ray system, Model NL5000, all NL5000 systems with software version before 05.01.01 - Product Usage: is inte...
Medical Devices·35 affected·Jul 15, 2020
High RiskFDA
Neurologica Corporation
WS80A Diagnostic Ultrasound System Version 1.00.16, 3.00.17, 3.00.18, 3.00.19, 3.01.00, 3.01.01, 3.01.02, 3.01.03, 3.01.04, 3.01.05, 3.01...
Diagnostic Devices·5,088 affected·Jul 25, 2019
High RiskFDA
Neurologica Corporation
HS70A Diagnostic Ultrasound System Version 2.01.00, 2.01.01, 2.01.02, 2.01.03, 2.01.04, 2.01.05, 2.01.06, 1.00.06, 1.00.07, 1.00.08, 1.00...
Diagnostic Devices·3,582 affected·Jul 25, 2019
High RiskFDA
Neurologica Corporation
Samsung GM85 Mobile Digital X-ray Imaging System Product Usage: The GM85 Digital X-ray imaging System is intended for use in generat...
Medical Devices·288 affected·May 6, 2019
High RiskFDA
Neurologica Corporation
The GC80 Digital X-ray Imaging System
Medical Devices·45 affected·Jun 22, 2017
High RiskFDA
Neurologica Corporation
Samsung GU60A system- Digital X-ray Imaging Systems are intended for use in generating radiographic images of human anatomy by a qualifi...
Medical Devices·87 affected·May 24, 2017