RecallHawk

BABESIDE Doll and Stroller Toys

Huizhou Huitong Crafts Co. Ltd., of China

Summary

CPSC recall: BABESIDE Doll and Stroller Toys. By Huizhou Huitong Crafts Co. Ltd., of China. Hazard: The recalled toys violate the small parts ban because they are intended for children under three and the small pacifier poses a deadly choking hazard to young children. In addition, the eyes on the plush bear can detach, also posing a choking hazard.. Remedy: Consumers should stop using the recalled toys' plush bear and pacifier immediately, take them away from children and contact HYBDOLLS for fr

Details

Source

CPSC Consumer Product Recall

External ID

10822

Action Date

2026-06-18

Status

Recalled

Category

consumer_product

Product Description

This recall involves BABESIDE-branded doll and stroller toys. The play toy sets consist of a pink with red stroller, a b

Context & Analysis

This is a unclassified recall.

This was one of 25 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Huizhou Huitong Crafts Co. Ltd., 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 (Huizhou Huitong Crafts 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 Huizhou Huitong Crafts Co. Ltd., of China have FDA actions?

Huizhou Huitong Crafts Co. Ltd., 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 "10822" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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