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CONAIR

CONAIR CORPORATION · Model NT11 · UDI-DI 00085452000693

JEQ
10
510(k) clearances
6,786
Adverse events
36
Recalls
358
Facilities

Description

ELECTRIC TOOTHBRUSH

Recalls

DateFirmReason
2026-05-21Papablic IncPotential for brush heads to break.
2026-05-21Papablic IncPotential for brush heads to break.
2013-12-18Ranir CorporationRanir, LLC is recalling all lots of UP & UP brand Kid's Power Toothbrush and TopCare brand Clifford Kids Power Toothbrush because the tufted disk may become detached from the power
2013-12-18Ranir CorporationRanir, LLC is recalling all lots of Up & Up brand Kid's Power Toothbrush and TopCare brand Clifford Kids Power Toothbrush because the tufted disk may become detached from the power
2011-12-22Church & Dwight IncChurch and Dwight plans to take actions to best convey to the public the potential small parts choking hazard with using a Spinbrush beyond the recommended 3-month brush head life.
2011-12-22Church & Dwight IncChurch and Dwight plans to take actions to best convey to the public the potential small parts choking hazard with using a Spinbrush beyond the recommended 3-month brush head life.
2011-12-22Church & Dwight IncChurch and Dwight plans to take actions to best convey to the public the potential small parts choking hazard with using a Spinbrush beyond the recommended 3-month brush head life.
2011-12-22Church & Dwight IncChurch and Dwight plans to take actions to best convey to the public the potential small parts choking hazard with using a Spinbrush beyond the recommended 3-month brush head life.
2011-12-22Church & Dwight IncChurch and Dwight plans to take actions to best convey to the public the potential small parts choking hazard with using a Spinbrush beyond the recommended 3-month brush head life.
2011-12-22Church & Dwight IncChurch and Dwight plans to take actions to best convey to the public the potential small parts choking hazard with using a Spinbrush beyond the recommended 3-month brush head life.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.