RecallHawk

Summary

CPSC recall: RootStim Beard Growth Serum, 5% Minoxidil. By Ronghui Intelligent Manufacturing Technology (Guangzhou) Co., Ltd., of China. Hazard: The beard growth serum contains minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The serum's packaging is not child-resistant, posing a risk of serious injury or death from poisoning if the contents are swallowed by young children.. Remedy: Consumers should immediately secure the recalled serum b

Details

Source

CPSC Consumer Product Recall

External ID

10565

Action Date

2026-01-15

Status

Recalled

Category

consumer_product

Product Description

This recall involves RootStim Beard Growth Serums spray bottles. The serums come in black boxes with orange and white le

Context & Analysis

This is a unclassified recall.

This was one of 27 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Ronghui Intelligent Manufacturing Technology (Guangzhou) 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 (Ronghui Intelligent Manufacturing Technology (Guangzhou) 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 Ronghui Intelligent Manufacturing Technology (Guangzhou) Co., Ltd., of China have FDA actions?

Ronghui Intelligent Manufacturing Technology (Guangzhou) 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 "10565" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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