Reported Sep 25, 2024 · Ongoing

Seer Home System is an ambulatory electroencephalograph (EEG) system intended for at-home use for extended EEG and…

Seer Medical Pty Ltd.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: SEER MEDICAL PTY LTD · 278-284 Queensberry St · Melbourne · N/A

Is this the product you have?

  • 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).
Lot codes and dates

7 of 7 products

Products covered by this recall
Model / numberBarcodesProduct as published
SM-03-8001-INT09355751001037UDI-DI: 09355751001037; Serial Numbers: 000089, 000090, 000091, 000092, 000095, 000182, 000201, 000207, 000208, 000211, 000225, 000245, 000258, 000259, 000285, 000286, 000289, 000290, 000291, 000292, 000296, 000297, 000298, 000299, 000301, 000305, 000307, 000308, 000309, 000310, 000312, 000313, 000316, 000321, 000322, 000323, 000094, 000183, 00028, 000302, 000303, 000306, 000311.
SM-01-800109355751001020UDI-DI: 09355751001020; Serial Numbers: 000074, 000084, 000113, 000118, 000119, 000187, 000188, 000191, 000223, 000224, 000225, 000226, 000228, 000229, 000230, 000232, 000239, 000241, 000242, 000243, 000244, 000245, 000247, 000250, 000251, 000259, 000262, 000263, 000277, 000279, 000280, 000282, 000283, 000286, 000287, 000288, 000289, 000290, 000291, 000292, 000294, 000297, 000299, 000300, 000301, 000302, 000303, 000304, 000305, 000306, 000307, 000308, 000309, 000310, 000312, 000313, 000315, 000317, 000318, 000319, 000320, 000321, 000322, 000323, 000324, 000327, 000328, 000329, 000333, 000335, 000336, 000337, 000339, 000340, 000341.
09355751001136Product Number: Monitoring Portal; UDI-DI: 09355751001136; Serial Numbers: DMPD80RCMDFX, DMPFRRE7Q1GJ, DMPFT3PDQ1KQ, DMPFT43HQ1GG, DMPFT46JQ1KQ, DMPFT4CYQ1KQ, DMPFT4X1Q1KQ, DMPFV0HGQ1KQ, DMPFV178Q1KQ, DMPFV19SQ1KQ, DMPFV1AFQ1KQ, DMPFV1AXQ1KQ, DMPFV1DBQ1KQ, DMPFV1KQQ1KQ, DMPFV1L2Q1KQ, DMPFV1LNQ1KQ, DMPFV1PRQ1KQ, DMPFV1Q8Q1KQ, DMPFV1R2Q1KQ, DMPFV1R9Q1KQ, DMPFV1SRQ1KQ, DMPFV1TEQ1KQ, DMPFV1WYQ1KQ, DMPFV1YGQ1KQ, DMPFV1ZBQ1KQ, DMPFV1ZMQ1KQ, DMPFV20DQ1KQ, DMPFV20PQ1KQ, DMPFV219Q1KQ, DMPFV21GQ1KQ, F9FF60LYQ1KQ, F9FF70Z5Q1KQ, F9FF71PAQ1KQ, F9FFQ413Q1GJ, F9FFQC4WQ1GG, F9FFQF9VQ1GG.
SM-01-900509355751001112UDI-DI: 09355751001112; Serial Number: 006240129.
SM-07-800109355751001129UDI-DI: 09355751001129; Serial Numbers: 007230809, 007230810, 007230823, 007230825, SM-07-9001_230829, 007231004, 007231005, 007231012, 007231023, 007231025, 007231102, 007231108, 007231109, 007231115, 007231120, 007231124, 00720240129, 00720240205, 00720240207, 00720240314, 007240318, 007240319, 007240327, 007240325, 007240326, 007240402, 007240403, 007240507, 007240515, 007240516, 007240522, 007240527, 007240531, 007240612, 007240613, 007240624, 007240626, 007240627, 007240628, 007240702, 007240703.
SM-01-9003-US09355751001099UDI-DI: 09355751001099; Serial Numbers: 230525, 004230609, 004230913, 004231121, 004240306, 004240403, 004240424, 004240502, 004240509, 004240531, 004240603, 004240626, 004240705.
SM-01-900809355751001105UDI-DI: 09355751001105; Serial Numbers: 00223058, 00223059, 00223066, 00224008, 00224011, 00224013, 00224017, 00224018, 00224021.
Amount recalled
3,948 units

Where it was sold

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:38 PM UTC

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