# Major Recall Alert: PRO-Fluoxetine 10 mg Capsule Recalled Due to Excess N-Nitroso-Fluoxetine Levels
Pro Doc Limitée has issued a recall for their **PRO-Fluoxetine 10 mg capsules** due to a serious safety concern. The affected lots may exceed the interim acceptable intake limit for **N-nitroso-fluoxetine**, a nitrosamine impurity that may pose health risks if consumed in excess over time. If you use this product, it’s essential to understand the impact of this recall and take immediate action. Keep reading for all the key details.
## Why This Recall is Important
Nitrosamines, including N-nitroso-fluoxetine, are chemical compounds that are classified as probable human carcinogens. Prolonged exposure to elevated levels of nitrosamines could potentially increase the risk of cancer. Health Canada has set interim acceptable intake limits for N-nitroso-fluoxetine to protect consumers, and the recalled lots of **PRO-Fluoxetine 10 mg capsules** may exceed these limits.
Fluoxetine, commonly used to treat depression, obsessive-compulsive disorder, and other mental health conditions, is a critical medication for many individuals. For those depending on these capsules, this recall underscores the importance of ensuring the safety of any pharmaceuticals you consume.
## Details of the Recall
Here’s what you need to know about the **PRO-Fluoxetine 10 mg capsule** recall:
- **Brand**: Pro Doc Limitée
- **Product Name**: PRO-Fluoxetine 10 mg capsule
- **Issue**: Certain lots of this product may exceed the interim acceptable intake limit for N-nitroso-fluoxetine.
- **Category**: Health risk – Potential exposure to unacceptable levels of nitrosamine impurities.
- **Date Announced**: October 17, 2023
- **Images of Packaging**: 
For more information, visit the official recall notice from Health Canada here: [Health Canada Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/pro-fluoxetine-10-mg-capsule-may-exceed-interim-acceptable-intake-limit-n-nitroso).
## What You Should Do
Taking action promptly and correctly is critical when a medication recall is announced. Here’s what you can do:
- **Stop using the product immediately.** If you have a bottle of **PRO-Fluoxetine 10 mg capsules**, stop taking it and confirm whether it’s part of the affected lots.
- **Check with your pharmacist or healthcare provider.** They can help determine if your product is part of the recall and suggest alternative medications if needed.
- **Contact the manufacturer if necessary.** For further guidance or questions, reach out to Pro Doc Limitée to report any adverse reactions or quality concerns related to this product.
- **Properly dispose of the recalled medication.** Follow local guidelines for medication disposal to ensure you safely eliminate recalled capsules.
Patients relying on fluoxetine should speak with healthcare professionals before stopping treatment to discuss suitable alternatives or adjustments to their medical routine.
## Stay Safe – Get Instant Recall Alerts
To stay informed about product recalls that could affect your health, download the **MyRecalls App** today. This user-friendly app offers instant notifications for recalls related to medications, food, and consumer goods in Canada, helping you protect yourself and your family. Besides real-time alerts, the app provides essential recall details, safety measures, and easy access to verified sources so you can act quickly in emergencies.
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By staying updated and taking preventative action, you can minimize potential risks and maintain your peace of mind.
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The safety and health of consumers are paramount, and this recall highlights the importance of vigilance when it comes to medications. For more information on this recall and future alerts, keep following trusted sources like **Health Canada** and reliable recall platforms.