Anzmtosn Magnet Fidget Spinner Sets
Summary
CPSC recalled Anzmtosn Magnet Fidget Spinner Sets by Shenzhenshibangduoladianzikejimaoyi Co., Ltd. (Shenzhen Bangduola Electronic Technology Trade Co., Ltd.), of China. Hazard: The recalled magnet spinner sets violate the mandatory standard for toys because the sets contain loose magnets, posing an ingestion hazard to children. When high-powered magnets are swallowed, they can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.. Remedy: Consumers should stop using the recalled magnetic fidget spinner sets immediately, take them away from children and dispose of them. To receive a full refund, consumers should send a photo of the disposal to Anzmtosn via email at Anzmtosn53@163.com..
Details
Source
cpsc
External ID
26104
Action Date
2025-11-20
Status
Ongoing
Category
product
Product Description
This recall involves Anzmtosn Magnet Fidget Spinner Sets. Each set contains 15 pieces and comes with four iridescent oval-shaped magnets, eight iridescent cuboidal-shaped magnetic stones, one red and yellow disk-shaped metal fidget spinner, one winged metal fidget spinner, and one multicolored infinity fidget cube. The set comes with a black fabric-lined storage case. The batch number, CCA06582, is printed on the back label of the packaging.
Context & Analysis
Shenzhenshibangduoladianzikejimaoyi Co., Ltd. (Shenzhen Bangduola Electronic Technology Trade Co., Ltd.), of China has 2 FDA actions in our database.
Frequently Asked Questions
How often does Shenzhenshibangduoladianzikejimaoyi Co., Ltd. (Shenzhen Bangduola Electronic Technology Trade Co., Ltd.), of China have FDA actions?
Shenzhenshibangduoladianzikejimaoyi Co., Ltd. (Shenzhen Bangduola Electronic Technology Trade Co., Ltd.), of China has 2 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.
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