RecallHawk

Lolanta children's hooded flannel bathrobes

Nanchang Zhongcangjishi E-commerce Co. Ltd, of China

Summary

CPSC recall: Lolanta children's hooded flannel bathrobes. By Nanchang Zhongcangjishi E-commerce Co. Ltd, of China. Hazard: The recalled children's bathrobes violate federal flammability regulations for children's sleepwear, posing a risk of burn injuries to children.. Remedy: Consumers should immediately take the recalled bathrobes away from children, stop using them and contact Nanchang Zhongcangjishi E-commerce for a full refund. Consumers should destroy the garments by cutting them in half an

Details

Source

CPSC Consumer Product Recall

External ID

9850

Action Date

2024-02-08

Status

Recalled

Category

consumer_product

Product Description

This recall involves two styles of 100% polyester hooded children's bathrobes; the dinosaur style in green, rose red and

Context & Analysis

This is a unclassified recall.

This was one of 19 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Nanchang Zhongcangjishi E-commerce 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 (Nanchang Zhongcangjishi E-commerce 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 Nanchang Zhongcangjishi E-commerce Co. Ltd, of China have FDA actions?

Nanchang Zhongcangjishi E-commerce 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 "9850" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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