Natus Neurology DBA Excel Tech., Ltd. (XLTEK)
Complete recall history across all FDA and CPSC categories — 7 total recalls
Natus Neurology DBA Excel Tech., Ltd. (XLTEK) appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Device Recalls (7)
FDA medical device enforcement actions by Natus Neurology DBA Excel Tech., Ltd. (XLTEK)
| Date | Product | Reason | Class |
|---|---|---|---|
| Jun 18, 2025 | Natus Brain Monitor Breakout Box, Part Number 021911; full-montage standard e... | Natus received two complaints of left side labeling show impedance for right ... | Class II |
| May 7, 2025 | Brand Name: OBM00002 OBM DAB (Digital Acquisition Box) Product Name: OBM0000... | Electrode placement labels on the Digital Acquisition Box (DAB) were applied ... | Class II |
| Dec 2, 2021 | IPELA FHD PTZ TILE KITS with Axis cameras used in combination with Natus Neur... | Tile kits that allow one to install and situate a video camera within a patie... | Class II |
| Mar 5, 2020 | natus newborn care Olympic Brainz Monitor, REF OBM00002. electroencephalograph | The OBM system functional test (impedance and noise) was not carried out on t... | Class II |
| May 18, 2018 | Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Export For ... | Natus Neuro has discovered a possible manufacturing defect in the ErgoJust mo... | Class II |
| May 15, 2018 | XLTEK EMU40EX EEG Headbox | Possible degradation of an internal electronic component over time which may ... | Class II |
| Nov 11, 2015 | Natus Quantum System with NeuroWorks Software. Catalog /Part Numbers: 013926.... | During an internal testing, Natus Medical Incorporated, identified that in Ne... | Class II |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
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