RCRecallCheck

Official recall atom

Pannonfitt — Laser therapy device — Family Laser

Official fact2026-06-12EU Safety GateMaterialised slice

Results are official records from named sources. Coverage is incomplete. This site is not medical advice and does not publish drug labels, openFDA, Prop 65 or NIH DSLD records.

Official action

Source. EU Safety Gate

Official identifier. OR/00073/26

Date. 2026-06-12

Jurisdiction. Hungary

Hazard (official). 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.

Action / remedy (official). Type of economic operator to whom the measure(s) were ordered: ImporterCategory of measure(s): Withdrawal of the product from the marketDate of entry into force: 23/06/2025Type of economic operator to whom the measure(s) were ordered: ImporterCategory of measure(s): Recall of the product from end usersDate of entry into force: 23/06/2025

Brand (official or joined product row). Pannonfitt

Model. CDU23, JG044961

Official record

Licence: European Commission Safety Gate reuse notice

Attribution: Alerts from the Rapid Alert System for dangerous non-food products, published free of charge on the Safety Gate website © European Union; use the current year range in the source disclaimer

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