# Major Recall Alert: Preime Dermafacial Recalled Due to Improper Classification and Missing Medical Device License
On June 30, 2025, Canadian health authorities announced the recall of **Preime Dermafacial**, a popular skincare device, due to regulatory compliance concerns. While the product itself has no defects, it was incorrectly sold as an electronic device when it should have been designated as a **Class II/Class III medical device**. As a result, it does not hold the required **Medical Device License (MDL)** for sale in Canada.
Consumers should take note of this important recall to ensure compliance with medical device regulations and protect themselves against potential future misuse. Read on to learn more about the recall, why it matters, and how to stay informed.
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## Why This Recall is Important
The **Preime Dermafacial recall** is not due to any defects or safety risks in the device itself, but rather a regulatory issue. It highlights the importance of proper classification and licensing for products marketed as medical devices.
### Here’s why this recall matters:
- Products inaccurately classified as non-medical devices bypass stringent health and safety checks required for medical devices in Canada.
- Class II/Class III medical devices, like Preime Dermafacial, typically require additional testing and licensing to ensure their safety and efficacy.
- By addressing this regulatory oversight, health authorities aim to maintain strict standards for consumer protection.
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## Details of the Recall
Stay updated on all the key details regarding this recall:
- **Product Name**: Preime Dermafacial
- **Brand**: Preime Dermafacial
- **Recall Reason**: The device was sold as an electronic device instead of a Class II/Class III medical device, meaning it lacks a valid **Medical Device License (MDL)** as required in Canada. It is important to note there are no defects present in the product.
- **Recall Start Date**: June 30, 2025
- **Image of Product**:

- **Official Source**: [Canada Recall Website](https://recalls-rappels.canada.ca/en/alert-recall/preime-dermafacial)
If you or someone you know owns the Preime Dermafacial device, it’s essential to take the next steps outlined below.
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## What You Should Do
If you purchased a **Preime Dermafacial device**, health authorities and consumer safety groups recommend the following:
- **Stop using the device** until further notice or until the manufacturer provides updated guidance.
- **Contact the seller or manufacturer** to inquire about returns, refunds, or reclassification updates.
- Check for updates on the official Canada recall site [here](https://recalls-rappels.canada.ca/en/alert-recall/preime-dermafacial).
- Keep a record of your purchase and any communication with the seller for future reference.
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By understanding the significance of medical device licensing and acting quickly on critical recalls, Canadian consumers can stay protected and informed. Keep an eye on the latest updates regarding the Preime Dermafacial recall to ensure your compliance and safety.