Electricalelectric shock

Fixed lamp (LUMINEX) · RENO

A live wire is in contact with the metal casing of the lamp. 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, nor…

Read the official notice → Fixed lamp
Date
2025-04-25
Country
Poland
Brand
Luminex
Product
Fixed lamp
Classification
electric shock
Category
Electrical
Source
EU Safety Gate

Copied automatically from the European Commission's Safety Gate. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the brand, model, batch number and pictures against the official notice.
  2. If yours matches, stop using it and keep it away from children.
  3. Follow the remedy in the notice: a refund, repair or replacement from the seller or maker. Many recalls also apply to items bought online.

General guidance from Recall Atlas. The official notice from the European Commission's Safety Gate has the exact models, batch codes and remedy, and it takes priority.

More Luminex recalls

  1. 2025-06-11
  2. US
    Drugs & medicalClass II

    Luminex Corporation recalls VERIGENE Gram Negative Blood Culture (BC-GN) Nucleic Acid Test, REF 20-006-021; for use with the sample-to-results VERIGENE System;…

    It was determined that the consumable issue may result in No Call - INT CTL 1 and/or False Negative results on a small portion of the lot of test cartridges.

    FDA · DeviceLuminex CorporationUS Nationwide distribution in the states of AL, CA, MN, TX, AZ, NJ, WA, SC,…Official notice →
  3. 2024-08-14
  4. US
    Drugs & medicalClass II

    Luminex Corporation recalls Verigene Gram Positive Blood Culture (BC-GP) Nucleic Acid Test

    Potential for defective test cartridges which may result in false positive results for the Staphylococcus lugdunensis and Enterococcus faecium targets.

    FDA · DeviceLuminex CorporationUS Nationwide distribution including in the states of AZ, CA, CO, DE, FL, GA,…Official notice →
  5. 2023-12-13
  6. US
    Drugs & medicalClass II

    Luminex Corporation recalls Luminex VERIGENE BC-GP Utility Tray (5-Pack Carrier), Gram-Positive Blood Culture Nucleic Acid Test, REF 20-011-018, a component of the…

    Potentially defective utility trays in the reagent kits.

    FDA · DeviceLuminex CorporationWorldwide - US Nationwide distribution in the states of AZ, CA, CO, DE, FL,…Official notice →
  7. 2023-07-05
  8. US
    Drugs & medicalClass II

    Luminex Corporation recalls VERIGENE Clostridium difficile Nucleic Acid Test, REF 30-002-022

    It is possible that in rare instances the VERIGENE CDF Nucleic Acid Test Kit (Part No. 20-005-022) and the VERIGENE Enteric Pathogens Nucleic Acid Test Kit (Part No. 20-005-023) could provide a false-negative result…

    FDA · DeviceLuminex CorporationWorldwide and US Nationwide DistributionOfficial notice →
  9. 2022-11-02
  10. US
    Drugs & medicalClass II

    Luminex Corporation recalls ARIES SARS-CoV-2 Assay, REF: 50-10047

    A part defect with the wash 1 syringe of an SARS-CoV-2 assay could lead to incomplete extraction thereby producing an invalid or false negative assay result.

    FDA · DeviceLuminex CorporationDistribution US nationwide, Indonesia, and Hong Kong.Official notice →
  11. 2022-08-24
  12. US
    Drugs & medicalClass II

    Luminex Corporation recalls ARIES SARS-CoV-2 Assay

    SARS-CoV-2 assay that detects SARS-CoV-2 ORF1ab and N genes may not detect the ORF1ab gene. A positive results if either SARS-CoV-2 genes is detected, but If both genes are mistakenly not detected, a false negative…

    FDA · DeviceLuminex CorporationU.S. Nationwide distribution in the states of NE, TX, MS, TN, KY, ME, CA.Official notice →
All 13 Luminex recalls →

Other electrical recalls in Poland

  1. 2025-06-06
  2. PLEU
    Electricalelectric shock

    Ceiling lamp · Lamps chandeliers

    The wires are protected with basic insulation only and are in contact with metal parts of the luminaire. In case of insulation damage live parts may become accessible, leading to a risk of electric shock. The product…

    EU Safety Gate · reported by PolandOfficial notice →
  3. PLEU
    Electricalelectric shock

    Ceiling lamp

    The wire opening on the product has sharp edges and the power supply cable could be damaged giving access to live parts. Moreover, the metal parts of the luminaire are not permanently connected to the earthing…

    EU Safety Gate · reported by PolandOfficial notice →
  4. 2025-05-23
  5. PLEU
    Electricalenvironment

    USB charger (Tel1) · Smart Travel Charger

    The product has an excessive concentration of lead (measured value up to 59.1% by weight). Lead poses a risk to the environment. The product does not comply with the requirements of the Directive on the restriction of…

    EU Safety Gate · reported by PolandTel1Official notice →
  6. 2025-03-28
  7. PLEU
    Electricalelectric shock

    Fixed lamp (Sigma) · Zoom

    A live wire is in contact with the metal casing of the lamp. 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, nor…

    EU Safety Gate · reported by PolandSigmaOfficial notice →
  8. 2025-02-07
  9. PLEU
    Electricalelectric shock

    LED light (Anlux)

    The insulation of the light is inadequate, making live parts accessible. The user can therefore receive an electric shock The product does not comply with the requirements of the Low Voltage Directive nor with the…

    EU Safety Gate · reported by PolandAnluxOfficial notice →
  10. 2025-01-17
  11. PLEU
    Electricalenvironment

    USB charger (REBEL) · POWER CHARGER

    The solders have an excessive concentration of lead (measured value up to 47.7%). Lead poses a risk to the environment. The product does not comply with the requirements of the Directive on the restriction of the use…

    EU Safety Gate · reported by PolandREBELOfficial notice →
See all electrical recalls →