Laser therapy device Recall – EU Safety Gate

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Published by Reclia Safety Desk | July 14, 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

Here is the factual recall information record based on the provided EU Safety Gate data.

Recall Information Record
Database: Consumer Safety (EU Safety Gate)
Record ID: OR/00073/26
Date of Record: 23/06/2025

1. Recall Summary
The notifying country of Hungary has issued a recall for the “Family Laser” low-level laser therapy device, manufactured by Pannonfitt. The recall was ordered due to a non-compliance risk involving burns. The product’s battery management system lacks a cell temperature monitoring device, which can cause the product to overheat. The product does not comply with the requirements of the Low Voltage Directive nor with the European standards EN 62133 and EN 60335. The economic operator (importer) has been ordered to withdraw the product from the market and recall the product from end users, effective 23/06/2025.

2. Affected Products
– Product: Laser therapy device (Low-level laser therapy device for home use)
– 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
– Notifying Country: Hungary
– Product Description: The device is a handheld unit intended for home use. It includes a USB charging cable and a pair of protective glasses. The device is stored in a blue, zippered, hard-shell carrying case.
– Production Dates: Not specified in the recall notice.

3. Hazard Information
– Risk Type: Burns
– Danger: The battery management system lacks a cell temperature monitoring device. As a result, the product can overheat and cause burns.
– Non-Compliance: The product does not comply with the requirements of the Low Voltage Directive nor with the European standards EN 62133 and EN 60335.
– Level: Other risk levels.

4. Consumer Action Required
Consumers who have purchased the “Family Laser” device (model CDU23, JG044961, batch GM202310144) should immediately stop using the product. The official measure ordered by the authorities is a recall of the product from end users. Consumers should follow the instructions provided by the importer regarding the return or disposal of the product. Specific instructions for consumers regarding how to return the product are not specified in the recall notice.

5. Official Remedy
The following measures were ordered by the authorities against the importer, effective 23/06/2025:
– Withdrawal of the product from the market: The product must be removed from all points of sale.
– Recall of the product from end users: Consumers are entitled to return the product. The specific remedy (e.g., refund, replacement, or repair) is not specified in the recall notice.

6. Contact Information
– Case Number: OR/00073/26
– Reference Link: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10099208
– Notifying Country: Hungary
– Company Recall Code: Not specified in the recall notice.
– URL for Recall: Not specified in the recall notice.
– Importer: The type of economic operator to whom the measures were ordered is the Importer. Specific contact details for the importer are not provided in the recall notice.

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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