The Recall Desk
Agency classClass IIOur severity:HighFDA (Devices)·Z-0858-2012·Announced 2012-08-08

Arm and Hammer Spinbrush Toothbrush Recalled for Choking Hazard

Church & Dwight is recalling Arm and Hammer Spinbrush toothbrushes due to a potential choking hazard from small parts if used beyond the recommended 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 0.731 million units of Arm and Hammer Spinbrush Dual Action Powered Toothbrush Pro Clean Re-Charge. The product was manufactured in China and distributed worldwide.

The recall is being conducted to convey to the public the potential small parts choking hazard associated with using the Spinbrush beyond the recommended 3-month brush head life. The toothbrush is intended for dental health and plaque removal.

Consumers should stop using the product if the brush head has exceeded its recommended 3-month life. The source text does not specify a specific consumer action such as returning the product or obtaining a refund, but notes the firm's intent to address the hazard communication.

The recalled product

Product
Arm and Hammer Spinbrush Dual Action Powered Toothbrush Pro Clean Re-Charge 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.

See all 10 products in this recall →

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