SEER MEDICAL PTY LTD: Device Recall
Recall #Z-3143-2024 · 08/12/2024
Recall Details
- Recall Number
- Z-3143-2024
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- SEER MEDICAL PTY LTD
- Status
- Ongoing
- Date Initiated
- 08/12/2024
- Location
- Melbourne, Australia
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 3,948 units
Reason for Recall
During CAPA investigations of sight production inconsistencies, it was highlighted that previous Electromagnetic Compatibility (EMC) assessments related to RF radiated emissions may not be reasonably equivalent to the current product due to design changes in the system. A new CAPA was opened to investigate the radiated emissions compliance issues. - Seer Home Systems distributed and retained in the field were not compliant with Electromagnetic Compatibility (EMC) testing according to IEC 60601-1-2 - Seer Home Systems, including accessories, were manufactured and distributed without application of proper design change and manufacturing controls - Seer Home Systems were distributed with labeling deficiencies
Product Description
Seer Home System is an ambulatory electroencephalograph (EEG) system intended for at-home use for extended EEG and video EEG (vEEG) recordings and analysis. The Seer Home System includes the Sight Monitoring Hub, the Sense wearable, Monitoring Portal and associated accessory components (Disposable EEG Wires, WaterTabs, WaterTabs Application Kit, and Take-home Kit).
Distribution Pattern
Worldwide - US Nationwide distribution in the states of MN, NY, PA and the countries of Australia.