Anzmtosn Luminous Fidget Spinner Balls
Summary
CPSC recall: Anzmtosn Luminous Fidget Spinner Balls. By Shenzhenshibangduoladianzikejimaoyi Co., Ltd (Shenzhen Bangduola Electronic Technology Trade Co., Ltd.), doing business as Anzmtosn, of China. Hazard: The recalled toys violate the?mandatory safety standard for toys?because the mini flashlight included with the fidget spinner balls contains button cell batteries that can be easily accessed by children. If button cell or coin batteries are swallowed, the ingested batteries can cause serious
Details
Source
CPSC Consumer Product Recall
External ID
10795
Action Date
2026-05-28
Status
Recalled
Category
consumer_product
Product Description
This recall involves Anzmtosn's Luminous Fidget Spinner Balls, Model FS0862. The model number is located on the back of
Context & Analysis
This is a unclassified recall.
This was one of 17 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.), doing business as Anzmtosn, 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.), doing business as Anzmtosn, 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.), doing business as Anzmtosn, of China in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10795" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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