Laser therapy device Recall – EU Safety Gate

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Published by Reclia Safety Desk | July 21, 2026

📌 EU Safety Gate Recall Notice

Product: Laser therapy device

Brand: Pannonfitt

Country: Hungary

Hazards: Fire Hazard, Electric Shock Hazard, Non-Compliance

What to do: Stop using this product. Follow the recall instructions for refund or replacement.

🇪🇺 Official EU Safety Gate Recall Notice
Case #OR/00073/26 |
View original notice →

Recall Summary

Product Laser therapy device
Brand Pannonfitt
Country Hungary
Case Number OR/00073/26
Hazard Fire Hazard, Electric Shock Hazard, Non-Compliance
Source 🇪🇺 EU Safety Gate

Reclia – Recall Information Database Record

Case Number: OR/00073/26
Notifying Country: Hungary
Date of Entry into Force of Measures: 23/06/2025

1. Recall Summary
The notifying country, Hungary, has issued a recall and market withdrawal for a laser therapy device. The product is a low-level laser therapy device intended for home use. The recall notice states that the battery management system lacks a cell temperature monitoring device. As a result, the product can overheat and cause burns. The product does not comply with the requirements of the Low Voltage Directive nor with the European standards EN 62133 and EN 60335. The measures were ordered by the authorities and apply to the importer.

2. Affected Products
– Product: Laser therapy device
– Brand: Pannonfitt
– Name: Family Laser
– Type/Model Number: CDU23, JG044961
– Batch Number: GM202310144
– Barcode: Not specified in the recall notice.
– Country of Origin: People’s Republic of China
– Description: Low-level laser therapy device for home use, including a USB charging cable and a pair of protective glasses. The handheld device is stored in a blue, zippered, hard-shell carrying case.
– Production Dates: Not specified in the recall notice.
– Company Recall Code: Not specified in the recall notice.

3. Hazard Information
The recall notice identifies the following hazard: The battery management system lacks a cell temperature monitoring device. The product can overheat and cause burns. The product does not comply with the requirements of the Low Voltage Directive nor with the European standards EN 62133 and EN 60335. The risk type is listed as “Burns.”

4. Consumer Action Required
The recall notice does not provide specific instructions for consumers regarding what they should do with the product. The official measure ordered by the authorities is the withdrawal of the product from the market and the recall of the product from end users. Consumers who possess this product should contact the importer or the retailer where the product was purchased for further instructions. The date of entry into force for these measures is 23/06/2025.

5. Official Remedy
The official remedy, as ordered by the authorities, consists of two measures:
– Withdrawal of the product from the market: The product is to be removed from retail shelves and distribution channels.
– Recall of the product from end users: The product is to be returned by consumers to the importer or retailer. The specific remedy for the consumer (e.g., refund, replacement, or repair) is not specified in the recall notice.

6. Contact Information
– Notifying Country: Hungary
– Case Number: OR/00073/26
– Reference URL: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10099208
– Importer: The type of economic operator to whom the measures were ordered is listed as “Importer.” The name and contact details of the importer are not specified in the recall notice.
– Retailer: Not specified in the recall notice.
– Consumer Contact: Not specified in the recall notice. Consumers are advised to contact the point of purchase or the importer for information regarding the return or remedy.

Recall Timeline

  • **Current** – Recall announced via EU Safety Gate
  • **Ongoing** – Consumers advised to stop using product
  • **Ongoing** – Refund or replacement available from manufacturer

Frequently Asked Questions

Q: How do I identify the recalled Laser therapy device?

A: Check the product label and packaging against the official EU Safety Gate recall notice (Case #OR/00073/26).

Q: What should I do if I own the recalled Laser therapy device?

A: The recall notice advises consumers to stop using the product immediately and follow the recall instructions.

Q: How do I get a refund or replacement for the recalled Laser therapy device?

A: Contact the manufacturer or retailer using the information in the recall notice.

Related EU Recalls (Click to expand)

Disclaimer: Information on this page is summarized from official EU Safety Gate recall notices.
Reclia is a recall information database and does not conduct product testing, safety certification,
or independent investigations.

Consumers should refer to the original EU Safety Gate notice
for complete details and official instructions.




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