NeuroLogica Corporation Recalls

All product recalls associated with NeuroLogica Corporation.

Get alerts for this brand

Recall Summary

Total Recalls

9

Past Year

1

Class I (Serious)

0

Most Recent

Oct 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–9 of 9 recalls

GM85 Digital Mobile X-ray System (NeuroLogica) – bolt fracture risk (2025)

The four (4) M5 bolts that secure the Tube Head Unit to the end of the arm may loosen or fracture due to metal fatigue.

Moderate

FDAOct 7, 2025Nationwide• NeuroLogica Corporation

GM60A X-Ray System (NeuroLogica) – Device Arm Fall Risk (2024)

Potential for the anti-fall system of the device arm to fail.

High

FDAJul 8, 2024Nationwide• NeuroLogica Corporation

Samsung Digital X-ray System (NeuroLogica) – Arm Welding Safety Issue (2023)

Mobile x-ray systems moving arm frame welding issue which presents the potential of bodily harm due to fall of the arm.

High

FDADec 28, 2023Nationwide

• NeuroLogica Corporation

OmniTom X-ray CT System (NeuroLogica) – Device Mobility Risks (2023)

1. Wheels loosening over time with use of the device could lead to the inability to effectively drive the device and could lead to delay in patient treatment. 2.Batteries used to power the NL5000 device contain contaminated boards, which may impact the ability to power on the device, this could lead to delay for patient treatment

Moderate

FDAJun 6, 2023Nationwide• NeuroLogica Corporation

Samsung GM85 X-ray System (NeuroLogica) – Arm Latch Safety (2023)

Issue related to the operation of the arm latch within the column that supports the arm, potential bodily harm due to a fall of the arm

High

FDAMar 8, 2023Nationwide• NeuroLogica Corporation

OmniTom CT X-Ray System (NeuroLogica) - Scanner Operational Fault (2020)

There are potential issues related to the operational state of the scanner, specifically for transport and inadvertent system shutdowns. There could be a possibility of potential delay in patient treatment if proper use instructions are not followed.

Moderate

FDAJul 15, 2020Nationwide• NeuroLogica Corporation

WS80A Diagnostic Ultrasound (NeuroLogica) – Probe Overheating Risk (2019)

There is a potential for probes overheating when decreasing the Doppler SV (Sample Volume) size value set by the user in the Doppler Only mode.

Moderate

FDAJul 25, 2019Nationwide• NeuroLogica Corporation

HS70A Diagnostic Ultrasound (NeuroLogica) – Probe Overheating Risk (2019)

There is a potential for probes overheating when decreasing the Doppler SV (Sample Volume) size value set by the user in the Doppler Only mode.

Moderate

FDAJul 25, 2019Nationwide• NeuroLogica Corporation

GM85 Mobile X-ray System (NeuroLogica) – Safety Latch Risk (2019)

Potential issue related to the operation of the safety latch within the column that supports the arm due to a possibility of potential bodily harm due to a fall of the arm in an unlikely event that the column wire breaks.

Moderate

FDAMay 6, 2019Nationwide• NeuroLogica Corporation

Stay Informed

NeuroLogica Corporation Recalls

Recall Summary

GM85 Digital Mobile X-ray System (NeuroLogica) – bolt fracture risk (2025)

GM60A X-Ray System (NeuroLogica) – Device Arm Fall Risk (2024)

Samsung Digital X-ray System (NeuroLogica) – Arm Welding Safety Issue (2023)

OmniTom X-ray CT System (NeuroLogica) – Device Mobility Risks (2023)

Samsung GM85 X-ray System (NeuroLogica) – Arm Latch Safety (2023)

OmniTom CT X-Ray System (NeuroLogica) - Scanner Operational Fault (2020)

WS80A Diagnostic Ultrasound (NeuroLogica) – Probe Overheating Risk (2019)

HS70A Diagnostic Ultrasound (NeuroLogica) – Probe Overheating Risk (2019)

GM85 Mobile X-ray System (NeuroLogica) – Safety Latch Risk (2019)