RecallHawk

Summary

CPSC recall: Arizer Solo II portable electronic vaporizer devices. By Specialty, health and wellness, and adult novelty stores nationwide and on arizer.com from June 2024 through July 2025 for about $170.. Hazard: The internal lithium-ion battery can overheat, produce smoke, and/or eject material, posing fire and burn hazards.. Remedy: Consumers should immediately stop using the Arizer Solo II portable vaporizers and contact 7111495 Canada for a free replacement. Customers whose serial number is

Details

Source

CPSC Consumer Product Recall

External ID

10406

Action Date

2025-09-18

Status

Recalled

Category

consumer_product

Product Description

This recall involves the Arizer Solo II, a portable electronic vaporizer device powered by an internal lithium-ion batte

Context & Analysis

This is a unclassified recall.

This was one of 12 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 June 2024 through July 2025 for about $170.) 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 June 2024 through July 2025 for about $170. 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 June 2024 through July 2025 for about $170. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "10406" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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