Product Wiki · Recalls · EU Safety Gate (RAPEX)

Girlanda — recall SR/02924/26

EU Safety Gate (RAPEX) · Finland · 2026-10-16 · 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
SR/02924/26
Date of alert
2026-10-16
Country / jurisdiction
Finland
Risk level
Serious risk
Risk type
Electric shock
Brand
spectrum LED / Wojnarowscy
Product category
Electrical appliances and equipment
Product type
Lighting chain
Barcode (EAN/GTIN)
5902650565159
🔴 Serious hazard — Reported risk: The live parts of the lamp cap are accessible when the lamp is partially screwed into the lampholder of the luminaire, leading to electric shock. Consequently, the user could touch accessible live parts and receive an electric shock. The product does not comply with the requirements of the Low Voltage Directive and the relevant European standard EN IEC 60598.
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 taking notified measure
Distributor
Category of measure
Recall of the product from end users
Date of entry into force
05/10/2026
Primary source: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10119318

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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.