RecallHawk

Summary

CPSC recall: Arizer Solo III portable electronic vaporizers (Intergalactic/Black color only). By Specialty, health and wellness and adult novelty stores nationwide and on Arizer.com from May 2025 through January 2026 for about $300.. Hazard: The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious injury or death to children from burns.. Remedy: Consumers should stop using the Arizer Solo III portable electronic vaporizers immediately and contact

Details

Source

CPSC Consumer Product Recall

External ID

10826

Action Date

2026-06-18

Status

Recalled

Category

consumer_product

Product Description

This recall involves the Arizer Solo III Intergalactic (Black), a portable electronic vaporizer powered by an internal l

Context & Analysis

This is a unclassified recall.

This was one of 25 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

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 (Specialty, health and wellness and adult novelty stores nationwide and on Arizer.com from May 2025 through January 2026 for about $300.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Specialty, health and wellness and adult novelty stores nationwide and on Arizer.com from May 2025 through January 2026 for about $300. have FDA actions?

This is the only FDA action we have on record for Specialty, health and wellness and adult novelty stores nationwide and on Arizer.com from May 2025 through January 2026 for about $300. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "10826" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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