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Ionostar plus and ionolux

Official notice

2 Feb 2024

Last checked

2 Feb 2024

Medium riskHealth Canada

An official Health Canada notice concerns Ionostar plus and ionolux. 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 Published 2024-02-02.

What to do now

Contact the manufacturer if you require additional information.

Recall number

75003

Official notice

2024-02-02

The hazard

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

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Recall Numbers

75003

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Affected products

Product 1

Affected products - Ionostar Plus, Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalog number - 2547 2543 2544 2549 2545 2548 2546

Product 2

Affected products - Ionolux, Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalog number - 2119 2118 2117 2120 2121 2124 2122 2123

Product 3

Affected products - Ionolux, Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalog number - 2115

Product 4

Affected products - Ionostar Plus, Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalog number - 2540

Risk / hazard

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

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Voco, Ionostar Plus And Ionolux.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

75003

Classification

Type II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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