Specialty, health and wellness and adult novelty stores nationwide and on Arizer.com from May 2025 through January 2026 for about $300. recalls
1 recall recorded since 2018, most recently on 18 June 2026. Status and classification are as published by the CPSC.
Recalls1
Ongoing (FDA)0
Terminated or completed0
Class I (FDA)0
Announced Consumer products
- Recall started
- 18 June 2026
- Reason
- 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 7111495 Canada regarding a replacement Solo III V2 unit. Consumers who register for the recall and have serial numbers confirmed to fall within the affected serial number ranges will receive instructions to dispose of the recalled device. Consumers will be asked to submit a photograph showing the word "recalled" written on their device in permanent marker and confirm that they have disposed of the device in accordance with applicable laws and regulations before receiving a replacement Solo III V2 unit. Note: Do not throw this recalled lithium-ion battery or device in the trash, the general recycling stream (e.g., street-level or curbside recycling bins), or used battery recycling boxes found at various retail and home improvement stores. Recalled lithium-ion batteries must be disposed of differently than other batteries, because they present a greater risk of fire. Your municipal household hazardous waste (HHW) collection center may accept this recalled lithium-ion battery or device for disposal. Before taking your battery or device to a HHW collection center, contact that office ahead of time and ask whether it accepts recalled lithium-ion batteries. If it does not, contact your municipality for further guidance.
- Recall number
- 26565
- Arizer Solo III portable electronic vaporizers (Intergalactic/Black color only)
CPSC recall notice
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.