FDA Device recall Z-2098-2012
Arm and Hammer Spinbrush Pro Clean Sonic Recharge Made in China
- FDA Device
- Class II
- terminated
- Published 2012-08-08
On 2012-08-08 the FDA classified a Class II recall of Arm and Hammer Spinbrush Pro Clean Sonic Recharge Made in China by Church And Dwight, citing church 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2098-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2011-12-22 |
| Published | 2012-08-08 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Church And Dwight |
| Distribution | n/a |
Product
Arm and Hammer Spinbrush Pro Clean Sonic Recharge Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal.
Reason
Church 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.
Identifiers
| code_info | N/A |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
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FDA Drug · Class I · 2025-07-09 · Church And Dwight
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2098-2012%22
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