FDA Device recall Z-0857-2012
Arm and Hammer Spinbrush Dual Action Powered Toothbrush Pro-Clean, various models
- 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 Dual Action Powered Toothbrush Pro-Clean, various models 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-0857-2012 |
| 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 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.
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-0857-2012%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.