RecallHawk

Mikario Trading 5-in-1 Convertible Baby Gyms

Ningbo Resoul Digital Technology Co., Ltd., of China

Summary

CPSC recall: Mikario Trading 5-in-1 Convertible Baby Gyms. By Ningbo Resoul Digital Technology Co., Ltd., of China. Hazard: The recalled baby gyms violate the mandatory safety standard for infant support cushions because the floor mats can obstruct an infant's breathing, posing a serious risk of injury or deadly suffocation hazard.. Remedy: Consumers should immediately stop using the baby gyms and contact Mikario Trading for a full refund. Consumers should remove the toy bar, cut the cushion in

Details

Source

CPSC Consumer Product Recall

External ID

10577

Action Date

2026-01-22

Status

Recalled

Category

consumer_product

Product Description

This recall involves Mikario Trading's 5-in-1 baby gyms. The recalled baby gyms convert from an activity center to a tum

Context & Analysis

This is a unclassified recall.

This was one of 22 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Ningbo Resoul Digital Technology 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 (Ningbo Resoul Digital Technology 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 Ningbo Resoul Digital Technology Co., Ltd., of China have FDA actions?

Ningbo Resoul Digital Technology 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 "10577" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for consumer_product

Related Actions