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Neurologica Corporation

Last updated May 23, 2026

Information

Country: US
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Catalogue (74)

Page 1 of 2

Device	Model / Reference	Registries	Class	Status
Option Assy, Omnitom Universal Transfer Board	0-00169-001	FDA UDI	Class II	Active
Ceretom Frazer Base Plate And Rails System	0-00157-001	FDA UDI	Class II	Active
Option, Stryker Procuity Bed Adapter	0-00204-001	FDA UDI	Class II	Active
Msu Stretcher	0-00192-001	FDA UDI	Class II	Active
Large Veterinary Platform	0-00173-001	FDA UDI	Class II	Active
CereTom Elite	0-NL3000-004	FDA UDI	Class II	Active
Linet Multicare Bed Adapter	0-00140-001	FDA UDI	Class II	Active
Stryker Bed Adapter	0-00149-001	FDA UDI	Class II	Active
Option, Or Table Adapter	0-00020-001	FDA UDI	Class II	Active
Option, Stryker Power Pro Ambulance Bed Adapter	0-00137-001	FDA UDI	Class II	Active
Option, Hill Rom Transtar Stretcher Adapter 19.5"	0-00026-001	FDA UDI	Class II	Active
Extended Universal Scan Board	0-00150-001	FDA UDI	Class II	Active
OmniTom Elite	0-NL5000-002	FDA UDI	Class II	Active
BodyTom 64	0-NL4100-001	FDA UDI	Class II	Active
Stryker Spirit 5700 Adapter	0-00185-001	FDA UDI	Class II	Active
Stryker Zoom Adapter	0-00029-001	FDA UDI	Class II	Active
Stryker Powerpro X Ambulance Scan Board W/ Latch Lock	0-00163-001	FDA UDI	Class II	Active
Water Phantom, 25 cm	10-01527-001	FDA UDI	Class II	Unknown
Pediatric Scanning Platform For Omnitom	0-00171-001	FDA UDI	Class II	Active
Scanner Drive System	0-00116-001	FDA UDI	Class II	Active
GMR40 Retrofit Kit	GMR40	FDA UDI	Class II	Active
Option, Nl4x00 Ws-240v	0-00132-003	FDA UDI	Class II	Active
Arjo Huntleigh Adapter	0-00187-001	FDA UDI	Class II	Active
Table Nl5000 Full Body Pediatric (fbpt)	0-00178-001	FDA UDI	Class II	Active
Huntleigh Enterprise Adapter	0-00102-001	FDA UDI	Class II	Active
OmniTom Elite PCD	0-NL5000-003	FDA UDI	Class II	Active
Hill-Rom Century Adapter	0-00048-001	FDA UDI	Class II	Active
CereTom	NL3000	FDA UDI	Class II	Active
Option, Pediatric Scanning Platform	0-00079-001	FDA UDI	Class II	Active
Option, Stryker In Touch Low Bed Adapter	0-00152-001	FDA UDI	Class II	Active
Option, Silhouette Scanboard With Target	0-00135-002	FDA UDI	Class II	Active
Option, Stryker S3 Bed Adapter	0-00141-001	FDA UDI	Class II	Active
Hill-Rom Advanta 2	0-00143-001	FDA UDI	Class II	Active
Flat Head Scan Board	0-00027-001	FDA UDI	Class II	Active
Option, Hill-Rom Totalcare Adapter	0-00117-001	FDA UDI	Class II	Active
Option, Extended Scanboard Long Post With Target	0-00202-001	FDA UDI	Class II	Active
HillRom Centrella	0-00181-001	FDA UDI	Class II	Active
Option Assy, Hill Rom Progressa Pulmonary Bed Adapter	0-00138-001	FDA UDI	Class II	Active
Adapter, Hill-Rom Care Assist Es Bed	0-00175-001	FDA UDI	Class II	Active
Stryker FOB Adapter	0-00086-001	FDA UDI	Class II	Active
Mobile ENT Computer Cart, Assembly	10-00159-001	FDA UDI	Class II	Active
Option Assy, Stryker In Touch Critical Care Bed Adapter	0-00087-001	FDA UDI	Class II	Active
Universal Scan Board	0-00135-001	FDA UDI	Class II	Active
Option Hill Rom Advanta Bed Adapter	0-00050-001	FDA UDI	Class II	Active
Option, Hill-Rom Progressa Pulmonary Scanboard With Target	0-00139-002	FDA UDI	Class II	Active
Option, Nl4x00 Ws-120v-S	0-00132-001	FDA UDI	Class II	Active
Ct Scanner, Nl4000	0-NL4000-001	FDA UDI	Class II	Active
Ct Scanner , Nl3000 Elite, Rail/Plate Config	0-NL3000-005	FDA UDI	Class II	Active
Option, Stryker Secure Adapter	0-00019-001	FDA UDI	Class II	Active
Option Plate Mounted Scanner	0-00080-001	FDA UDI	Class II	Active

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FDA Recalls (13)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Oct 7, 2025	Z-0480-2026	—	open, classified	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.
Jul 8, 2024	Z-2715-2024	—	open, classified	Potential for the anti-fall system of the device arm to fail.
Dec 28, 2023	Z-1056-2024	—	open, classified	Mobile x-ray systems moving arm frame welding issue which presents the potential of bodily harm due to fall of the arm.
Jun 6, 2023	Z-2068-2023	—	open, classified	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
Mar 8, 2023	Z-1414-2023	—	open, classified	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
Jul 15, 2020	Z-2772-2020	—	terminated	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.
Jul 25, 2019	Z-2276-2019	—	terminated	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.
Jul 25, 2019	Z-2275-2019	—	terminated	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.
May 6, 2019	Z-1691-2019	—	terminated	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.
Jan 12, 2018	Z-1391-2018	—	terminated	While transporting the portable machine with the retrofit equipment in a backwards motion, there is potential for foot injury from the underside of the detector bin of the retrofit unit.
Jun 22, 2017	Z-0726-2018	—	terminated	An image was obtained with over exposure during a Thorax examination using the AEC function.
May 24, 2017	Z-3036-2017	—	terminated	When performing the Stitching function on GU60A system, unintended area is exposed to radiation
Sep 14, 2015	Z-0263-2016	—	terminated	When the system is driving over a non-conductive floor and then over a conductive, grounded part, proper control of the drive behavior may not be possible. The system can be stopped by releasing the drive handle or by pressing the emergency switch. Proper behavior is re-enabled when the system is rebooted.