Recall Register

Natus Neurology DBA Excel Tech., Ltd. (XLTEK): FDA recalls

FDA enforcement reports name Natus Neurology DBA Excel Tech., Ltd. (XLTEK) as the recalling firm in 7 events. The events have 7 product records. The recalls started from 2015 to 2025. All the events are device recalls.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Enforcement events

7 events, newest first.

FDA enforcement events of Natus Neurology DBA Excel Tech., Ltd. (XLTEK)
InitiatedProduct (first record)TypeClassRecordsStatus
18 Jun 2025Natus Brain Monitor Breakout Box, Part Number 021911; full-montage standard electroencephalographDeviceClass II1Ongoing
7 May 2025Brand Name: OBM00002 OBM DAB (Digital Acquisition Box) Product Name: OBM00002 OBM DAB (Digital Acquisition Box) Model/Catalog Number: OBM00002 OBM DAB (Digital Acquisition Box) Software Version: N/A Product Description: OBM00002 OBM DAB (Digital Acquisition Box) Component: NoDeviceClass II1Ongoing
2 Dec 2021IPELA FHD PTZ TILE KITS with Axis cameras used in combination with Natus Neuroworks/Sleepworks softwareDeviceClass II1Terminated
5 Mar 2020natus newborn care Olympic Brainz Monitor, REF OBM00002. electroencephalographDeviceClass II1Terminated
18 May 2018Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Export For PTZ Video Ext, IP PTZ HD ErgoJust Video Extension, EuroJust ICU Cart Export For PTZ Video Ext. Video cart used for mobile medical record documentation.DeviceClass II1Terminated
15 May 2018XLTEK EMU40EX EEG HeadboxDeviceClass II1Terminated
11 Nov 2015Natus Quantum System with NeuroWorks Software. Catalog /Part Numbers: 013926. The Natus Quantum Amplifier is intended to be used as an electroencephalograph: to acquire, display, store and archive electrophysiological signals. The amplifier should be used in conjunction with Natus NeuroWorks /SleepWorks software to…DeviceClass II1Terminated

An event with 1 product record and a class that is not Class I has no page. It has a row in this table.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Recalling firm: The firm that the FDA record names for a recall.

Type and class

Natus Neurology DBA Excel Tech., Ltd. (XLTEK): events for each product type
TypeEvents
Device7
Natus Neurology DBA Excel Tech., Ltd. (XLTEK): events in each class
ClassEvents
Class II7
Share of the events of the firm in Class I
0%
Share of all events on the register in Class I
18%
Events with the status Ongoing
2

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Events by year

FDA enforcement events of Natus Neurology DBA Excel Tech., Ltd. (XLTEK), by the year that the recall started. The largest year is 2018, with 2 events.

Official channels

Cite this page

Recall Register. Natus Neurology DBA Excel Tech., Ltd. (XLTEK): FDA recalls. https://recallregister.com/firm/natus-neurology-dba-excel-tech-ltd-xltek/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
State of the firm address
N/A

The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.

A firm with more products can have more recalls. This site does not compare one firm with a different firm. How the register is made. Report an error.

Questions

Which classes do the FDA recalls of Natus Neurology DBA Excel Tech., Ltd. (XLTEK) have?
Class II: 7 events. The class is for the product of a recall. It is not a class of the firm.
What is the newest FDA recall of Natus Neurology DBA Excel Tech., Ltd. (XLTEK)?
FDA event 97091, which the firm started on 18 Jun 2025. The first product in the record is: Natus Brain Monitor Breakout Box, Part Number 021911; full-montage standard electroencephalograph
How many FDA recalls of Natus Neurology DBA Excel Tech., Ltd. (XLTEK) have the status Ongoing?
2 events have the status Ongoing in the openFDA file. openFDA says about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.