Severity
Moderate
CPSC recall · Reported June 18, 2026
The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious injury or death to children from burns.
The CPSC recalled This recall involves the Arizer Solo III Intergalactic (Black), a portable electronic vap… - a moderate-severity action.
Arizer Solo III Portable Vaporizers Recalled Due to Fire and Burn Hazards; Risk of Seriou… was recalled and listed by the CPSC in June 18, 2026. Reason: The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious inj…. Remedy: Consumers should stop using the Arizer Solo III portable electronic vaporizers immediatel…. Verify recall #26565 with the CPSC before acting.
The recall
issued this moderate-severity CPSC recall-The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious inj….
Sourced from official CPSC enforcement records. Verify recall #26565 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This CPSC action (record #26565) was formally reported on June 18, 2026. It is classified under Moderate severity, with a current status of Active. The recalling firm is not specified in the federal record. Federal records list the affected scope as About 5,000.
The documented reason for this recall is: The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious injury or death to children from burns. Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. The remedy documented by the agency is: 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 a… - consumers holding this product should act on that instruction rather than relying on general guidance.
Within the same product category the archive holds 6 closely related recalls, 5 from CPSC - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 40,422 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
About 5,000
Related Recalls
6
5 from same agency
This recall involves the Arizer Solo III Intergalactic (Black), a portable electronic vaporizer powered by an internal lithium-ion battery. The unit features a rigid anodized aluminum housing. It includes a front-facing digital display for temperature and device settings, with a stainless steel heating chamber and removable glass components. Only devices with serial numbers beginning with the following prefixes are included in this recall: The model number "C0001-NB 130-LCUS" is on a barcode sticker on the packaginM3B1G5 M3F4G6 M35C43 M3PN54 M3SR42 M38G53 M3G576 M3C121 The serial number is etched on the bottom of the device and is also printed on the outside of the product packaging. UPC 628078802274 is printed on the product packaging.
The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious injury or death to children from burns.
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.
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 26565 |
| Date reported | June 18, 2026 |
| Date initiated | June 18, 2026 |
| Recalling firm | Not disclosed |
| Affected scope | About 5,000 |
| Distribution | Not disclosed |
| Official source | CPSC notice → |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
What to do with this recall
Consumers should stop using the Arizer Solo III portable electronic vaporizers immediately and contact 7111495 Canada regarding a…
This page summarizes the official CPSC record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Source: FDA, CPSC, and NHTSA federal recall databases. This recall: CPSC, reported June 18, 2026.
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.