Product Wiki · Recalls · EU Safety Gate (RAPEX)

AUPO — Chemical products — recall A12/03081/24

EU Safety Gate (RAPEX) · Malta · 2024-11-08 · Serious risk

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked on this page. No AI-generated text appears on this page. How we use AI →
Agency
EU Safety Gate (RAPEX)
Recall identifier
A12/03081/24
Date of alert
2024-11-08
Country / jurisdiction
Malta
Risk level
Serious risk
Risk type
Chemical
Brand
AUPO
Product category
Chemical products
Product type
Disposable electronic cigarette
Barcode (EAN/GTIN)
6972551365225
Reported risk: The product has an excessive amount of nicotine-containing liquid (declared volume: 5 ml). This could lead to the accidental consumption of a high dose of nicotine. Nicotine is acutely toxic and can endanger the user’s safety, notably if the product comes into contact with the skin or is ingested. Additionally, the product labelling is misleading, and it does not contain information on its nicotine content, concentration and delivery dose. As a consequence, consumers cannot make informed decisions regarding the safe use of the product.
What to do

Check whether your product matches this notice (name, batch, dates). If it does, stop using it and follow the instructions in the official notice — refund, return, repair or disposal are set by the issuing authority and the business, and they differ per recall. Official notice from EU Safety Gate (RAPEX) →

Action taken by the authority
Type of economic operator to whom the measure were ordered
Other
Category of measure
Ban on the marketing of the product and any accompanying measures
Date of entry into force
15/10/2024
Type of economic operator taking notified measure
Importer
Primary source: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10091818

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.