Anzmtosn Magnet Fidget Spinner Sets
Summary
CPSC recall: 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,
Details
Source
CPSC Consumer Product Recall
External ID
10494
Action Date
2025-11-20
Status
Recalled
Category
consumer_product
Product Description
This recall involves Anzmtosn Magnet Fidget Spinner Sets. Each set contains 15 pieces and comes with four iridescent ova
Context & Analysis
This is a unclassified recall.
This was one of 16 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Frequently Asked Questions
What is a FDA recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Shenzhenshibangduoladianzikejimaoyi Co., Ltd. (Shenzhen Bangduola Electronic Technology Trade Co., Ltd.), of China) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Shenzhenshibangduoladianzikejimaoyi Co., Ltd. (Shenzhen Bangduola Electronic Technology Trade Co., Ltd.), of China have FDA actions?
This is the only FDA action we have on record for Shenzhenshibangduoladianzikejimaoyi Co., Ltd. (Shenzhen Bangduola Electronic Technology Trade Co., Ltd.), of China in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10494" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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