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PMS-Fluoxetine 10 mg capsule Recall Due to Affected lots may exceed the inter...

# Major Recall Alert: PMS-Fluoxetine 10 mg Capsule Recalled Due to Potentially Exceeding Limits for N-nitroso-fluoxetine

Pharmascience has issued an important recall affecting several lots of their PMS-Fluoxetine 10 mg capsules. The affected lots may exceed the interim acceptable intake limit for N-nitroso-fluoxetine, a potentially harmful impurity. If you or someone you know is taking this medication, here's what you need to know and the steps you should take.

## Why This Recall is Important

Fluoxetine is a widely used medication prescribed to treat conditions such as depression, obsessive-compulsive disorder, and anxiety. However, the presence of impurities like N-nitroso-fluoxetine is a significant concern. N-nitroso compounds are classified as probable human carcinogens, meaning that long-term exposure to excessive levels may increase the risk of cancer.

This recall is part of an ongoing effort by manufacturers to abide by strict health standards and safeguard patient safety. Improper quality control can have serious consequences, making it essential for consumers to take action immediately if their product is affected.

## Details of the Recall

Pharmascience has identified that specific lots of their PMS-Fluoxetine 10 mg capsules may contain N-nitroso-fluoxetine above the acceptable intake limit.

Here are the key details of this recall:
- **Category**: CAN - N-nitroso-fluoxetine levels may exceed acceptable limits.
- **Brand**: Pharmascience
- **Product**: PMS-Fluoxetine 10 mg capsules
- **Recall Reason**: Affected lots may have dangerously high levels of N-nitroso-fluoxetine above the interim limits.
- **Date Announced**: October 2023

Consumers can view the product image for reference [here](https://myrecalls.app/images/products/29170_1751400750.jpg).

For the official recall notice, click [here](https://recalls-rappels.canada.ca/en/alert-recall/pms-fluoxetine-10-mg-capsule-may-exceed-interim-acceptable-intake-limit-n-nitroso).

## What You Should Do

If you currently use PMS-Fluoxetine 10 mg capsules, here are the recommended steps to take:

- **Check the lot number**: Look at your product packaging to verify if it matches the affected lots mentioned in the recall notice.
- **Stop using the product**: If your product is part of the recall, discontinue use immediately.
- **Contact your pharmacist or healthcare provider**: Discuss alternative treatment options or replacement medications with your provider to avoid any gaps in therapy.
- **Return the product**: Return affected capsules to the pharmacy or retailer where you purchased them for proper disposal.

Remember, your health is a priority. If you have experienced any adverse effects while taking this medication, consult a healthcare professional as soon as possible.

## Stay Safe – Get Instant Recall Alerts

Pharmaceutical recalls like the one involving PMS-Fluoxetine 10 mg capsules highlight the importance of staying informed about product safety issues. To keep you and your loved ones safe:

- **Download the MyRecalls App**: Get instant alerts about recalls, including medications and other products, sent directly to your device. Stay one step ahead when it comes to protecting your health and well-being.

Keeping track of product recalls is essential, especially for those involving medications that may pose health risks. Be proactive—download the MyRecalls app today and never miss a critical alert!

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Protect your health and stay informed. For more information on this recall, visit the official government source [here](https://recalls-rappels.canada.ca/en/alert-recall/pms-fluoxetine-10-mg-capsule-may-exceed-interim-acceptable-intake-limit-n-nitroso).

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