Iristar Minoxidil Spray Bottles
Shaoshan Leiluo Trading Co., Ltd. of Shaoshan, Hunan of China
Summary
CPSC recall: Iristar Minoxidil Spray Bottles. By Shaoshan Leiluo Trading Co., Ltd. of Shaoshan, Hunan of China. Hazard: The recalled spray bottles contain minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The 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 spray bottles out of sight and reach
Details
Source
CPSC Consumer Product Recall
External ID
10576
Action Date
2026-01-22
Status
Recalled
Category
consumer_product
Product Description
This recall involves Iristar Minoxidil Spray Bottles, 5% minoxidil with biotin for hair and beard growth. The sprays com
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.
Shaoshan Leiluo Trading Co., Ltd. of Shaoshan, Hunan 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 (Shaoshan Leiluo Trading Co., Ltd. of Shaoshan, Hunan 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 Shaoshan Leiluo Trading Co., Ltd. of Shaoshan, Hunan of China have FDA actions?
Shaoshan Leiluo Trading Co., Ltd. of Shaoshan, Hunan 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 "10576" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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