Arm and Hammer Spinbrush Toothbrush Recalled for Choking Hazard
Church & Dwight is recalling 22.783 million Arm and Hammer Spinbrush toothbrushes worldwide due to a potential choking hazard from small parts.
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 High severity criteria.
Plain-English summary
Church & Dwight Inc. is recalling 22.783 million units of the Arm and Hammer Spinbrush Dual Action Powered Toothbrush Pro-Clean, various models. The products were manufactured in China 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 three-month brush head life. The agency classification for this recall is Class II.
Consumers should stop using the toothbrush if the brush head has exceeded the recommended three-month life to avoid the potential choking hazard.
The recalled product
- Product
- Arm and Hammer Spinbrush Dual Action Powered Toothbrush Pro-Clean, various models. 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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