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Ezcam intraoral camera

Official notice

7 Mar 2025

Last checked

7 Mar 2025

Medium riskHealth Canada

An official Health Canada notice concerns Ezcam intraoral camera. Importation and sale of an unlicensed class II medical device. Vatech America misclassified the EZCam Intraoral Camera as a class I medical device. Recall Start Date: March 1, 2025 Published 2025-03-07.

What to do now

Contact the manufacturer if you require additional information.

Recall number

77077

Official notice

2025-03-07

The hazard

Importation and sale of an unlicensed class II medical device. Vatech America misclassified the EZCam Intraoral Camera as a class I medical device. Recall Start Date: March 1, 2025

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

77077

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Affected products

Product 1

Affected products - EZCam Intraoral Camera, Lot or serial number - All lots., Model or catalog number - N/A

Risk / hazard

Importation and sale of an unlicensed class II medical device. Vatech America misclassified the EZCam Intraoral Camera as a class I medical device. Recall Start Date: March 1, 2025

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: Vatech, Ezcam Intraoral Camera.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

77077

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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