Disposable Subdermal Eeg Needle Electrode

Recall Summary Disposable Subdermal EEG Needle Electrodes are being recalled across Canada due to a mechanical defect. These electrodes are medical devices used to record brain activity during EEG procedures. The defect could affect the device's ability to function properly during use.

Product

Disposable Subdermal Eeg Needle Electrode

Reason

Mechanical defect

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2022-01-04

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/6bfc9bdf-a1ab-4f27-841f-a8e7463ec15c