Sanlebi Pet Vet Playsets
Guangzhou Letao Keji Youxiangongsi, doing business as Letokids, of China
Summary
CPSC recall: Sanlebi Pet Vet Playsets. By Guangzhou Letao Keji Youxiangongsi, doing business as Letokids, of China. Hazard: The Pet Vet Playset violates the mandatory standard for toys because the button cell batteries in the nail grinder and otoscope can be easily accessed by children.. Remedy: Consumers should take away the nail grinder and otoscope from children immediately, stop using them and remove and properly dispose of the batteries. Consumers will be asked to throw the nail grinder and
Details
Source
CPSC Consumer Product Recall
External ID
10713
Action Date
2026-04-16
Status
Recalled
Category
consumer_product
Product Description
This recall involves the Sanlebi Pet Vet Playset, model MX094. The playset includes 25 toy veterinary role-play parts in
Context & Analysis
This is a unclassified recall.
This was one of 37 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Guangzhou Letao Keji Youxiangongsi, doing business as Letokids, of China has 2 FDA actions in our database, including 1 recall.
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 (Guangzhou Letao Keji Youxiangongsi, doing business as Letokids, 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 Guangzhou Letao Keji Youxiangongsi, doing business as Letokids, of China have FDA actions?
Guangzhou Letao Keji Youxiangongsi, doing business as Letokids, of China has 2 FDA actions in our database, including 1 recall and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10713" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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