ProductGuru Recalls

Official recall record

Ionostar Plus and Ionolux

Health Canada — Medical Devices · 2024-02-02 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2024-02-02
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

Due to an error in the manufacturing process, it is possible that an incorrect plunger has been fitted to some capsules. This plunger does not contain the correct reactive component for Ionostar Plus. When these capsules are activated, curing is significantly delayed and incomplete. Processing according to the Instructions For Use (IFU) is not possible. The reactive component in the incorrect plungers contains small amounts of BHT and Methacrylate. These ingredients are not listed in the IFU. Recall Start Date: January 23, 2024

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

More recalls: Health Canada — Medical Devices · Canada · all filters

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