Recall company profile

Natus Neurology DBA Excel Tech., Ltd. (XLTEK) Recalls

Overview of recall records associated with Natus Neurology DBA Excel Tech., Ltd. (XLTEK), including dates, categories and classifications where available.

5recall records
Jun 18, 2025latest record date
Aug 8, 2018earliest record date

Recall history in this database

Classification mix: Class II: 5.

Medical DeviceJun 18, 2025

OBM00002 OBM DAB (Digital Acquisition Box) recall — FDA Z-1925-2025

Electrode placement labels on the Digital Acquisition Box (DAB) were applied backwards. This may ultimately lead to misdiagnosis of seizure location in neonates monitored with this device.

Class IIFDA: OngoingNatus Neurology DBA Excel Tech., Ltd. (XLTEK)
Medical DeviceAug 8, 2018

XLTEK EMU40EX EEG Headbox recall — FDA Z-2570-2018

Possible degradation of an internal electronic component over time which may cause the XLTEK EMU 40EX Breakout box to fail. It may feel hot and plastic case may start melting.

Class IIFDA: TerminatedNatus Neurology DBA Excel Tech., Ltd. (XLTEK)

Understanding this recall history

This page summarizes recall records in which the official source identifies Natus Neurology DBA Excel Tech., Ltd. (XLTEK) as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.