RecallHawk

RootStim 5% Minoxidil Foam Hair Regrowth Treatment with Rosemary and Biotin, RootStim Minoxidil Hair Regrowth Treatment

Unknown Manufacturer

Summary

CPSC recalled RootStim 5% Minoxidil Foam Hair Regrowth Treatment with Rosemary and Biotin, RootStim Minoxidil Hair Regrowth Treatment 5% Minoxidil Rosemary & Biotin and RootStim Minoxidil Hair Regrowth Treatment 5% Minoxidil with Rosemary by Unknown Manufacturer. Hazard: The recalled hair regrowth products contain minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The bottle is not child-resistant, posing a risk of serious injury or death from poisoning if the contents are ingested by young children.. Remedy: Consumers should secure the recalled products out of sight and reach of children immediately and contact RootStim for instructions on receiving a replacement product. Consumers will be asked to write “RECALLED” on the bottle, discard the bottle and send a photo of the discarded bottle to finergraceing@gmail.com..

Details

Source

cpsc

External ID

27058

Action Date

2026-10-29

Status

Ongoing

Category

product

Product Code

Containers,plastic,incl.bottles,bowls, Etc.

Product Description

This recall involves three RootStim Minoxidil Hair Regrowth Treatment bottles: RootStim 5% Minoxidil Foam Hair Regrowth Treatment with Rosemary and Biotin, 6 fl. oz. The Foam comes in a blue and white package, with an orange accent band or orange lettering. The package contains three 2 fl. oz. pump-foam bottles. UPC code 810169130594 is printed on a label on the bottom of the box. RootStim Minoxidil Hair Regrowth Treatment 5% Minoxidil Rosemary & Biotin, 2 fl. oz. The spray comes in a magenta box with a 2 fl. oz spray-pump bottle. UPC code 810169301005 is on a label on the bottom of box. RootStim Minoxidil Hair Regrowth Treatment 5% Minoxidil with Rosemary, 4 fl. oz. The serum comes in a blue and white package with an orange accent band containing two 2 fl. oz. amber glass bottles with black spray-pump caps. UPC code 810169301012 is on a label on the bottom of the box.

Context & Analysis

Unknown Manufacturer has 1466 FDA actions in our database.

Frequently Asked Questions

How often does Unknown Manufacturer have FDA actions?

Unknown Manufacturer has 1466 FDA actions in our database, including 0 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.

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