Lifelines Neuro recalls ElectroTek Temporal Sensor Cable Gold for potential incorrect electrode labels that could lead to EEG study errors. Affected units have specific model and lot codes.
Potential for one of the four temporal electrode cables used in with the ElectroTek EEG system having incorrect placement labels which could lead to incorrect placement of electrode for an EEG study.
Lifelines Neuro is recalling ElectroTek Temporal Sensor Cables due to possible incorrect placement labels on the cables. This could cause improper electrode placement during EEG studies, potentially leading to inaccurate results.
The cables have incorrect placement labels that might lead to electrodes being placed in the wrong position on a patient's scalp. This could cause inaccurate brain activity readings during EEG studies, but does not pose a direct physical risk to the user.
Healthcare professionals using the ElectroTek EEG system for brain activity studies may be affected. Patients undergoing EEG tests with this cable could face inaccurate results.
Check for model number PL00010-29.00-31.75.33.0:00-35.50-G and lot code J380188 on the cable packaging. The product was sold with the ElectroTek EEG system for brain activity studies.
Look for model number PL00010-29.00-31.75.33.00-35.50-G and lot code J380188 on the cable packaging.
The recall is for potential incorrect placement labels on the cables that could lead to improper electrode placement during EEG studies.
The model number is PL00010-29.00-31.75.33.00-35.50-G.
Check for model number PL00010-29.00-31.75.33.00-35.50-G and lot code J380188 on the cable packaging.
We’ve drafted a message you can send Lifelines Neuro to request your refund or repair — edit it as you like.
Subject: Recall Z-0722-2020 — Lifelines Neuro Lifelines Neuro Hello, I own a Lifelines Neuro that is covered by recall Z-0722-2020 from Lifelines Neuro. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
