Arm and Hammer Spinbrush Pro White Sonic Toothbrush Recalled for Choking Hazard
Church & Dwight is recalling Arm and Hammer Spinbrush Pro White Sonic Toothbrushes due to a potential choking hazard from small parts if used beyond the recommended 3-month brush head life.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a choking hazard, which is a risk-of-harm product where injury has not yet been reported, fitting the criteria for a High severity score.
Plain-English summary
Church & Dwight Inc. is recalling approximately 54,000 units of the Arm and Hammer Spinbrush Pro White Sonic Toothbrush. The product was manufactured in China for Church & Dwight Co., Inc. in Princeton, NJ, and distributed worldwide. The recall is being conducted to better convey to the public the potential small parts choking hazard associated with using the Spinbrush beyond the recommended 3-month brush head life.
The hazard involves small parts that may pose a choking risk if the toothbrush is used after the brush head has exceeded its recommended lifespan. The source text does not report any specific illnesses, injuries, or deaths associated with this recall. Consumers are advised to stop using the product if the brush head has been in use for more than three months to avoid the potential choking hazard.
The recalled product
- Product
- Arm and Hammer Spinbrush Pro White Sonic Toothbrush Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal
- Manufacturer
- Church & Dwight Inc
- Category
- Consumer Product — Personal Care
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- N/A
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 10 recalled by Church & Dwight Inc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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