# Major Recall Alert: Sandoz Fesoterodine Fumarate 8 mg Tablet Recalled Due to Out-of-Specification Diester Impurity
Health Canada has announced a recall of **Sandoz Fesoterodine Fumarate 8 mg tablets** due to the presence of a Diester impurity that exceeds acceptable specifications. If you or someone you know uses this medication, it’s crucial to understand the implications of this alert and take immediate action.
### Why This Recall is Important
Medications must meet strict safety and quality standards to ensure patient safety. The presence of an impurity, such as the **Diester impurity found in Sandoz Fesoterodine Fumarate**, poses potential health risks. Although no immediate adverse events have been reported to date, consuming products with out-of-specification impurities over time could lead to side effects or compromise treatment outcomes.
Fesoterodine Fumarate is commonly prescribed to treat overactive bladder (OAB) symptoms, including urgent or frequent urination. This recall signals a pressing concern for patients relying on this medication for quality of life and symptom management.
### Details of the Recall
The recall, issued on **28318**, applies specifically to certain lots of Sandoz Fesoterodine Fumarate 8 mg tablets. Below is a quick summary of the recall information:
- **Category**: CAN
- **Brand**: Sandoz Canada
- **Product**: Sandoz Fesoterodine Fumarate 8 mg tablets
- **Reason for Recall**: Out-of-specification levels of Diester impurity detected in affected lots
If your medication is part of the affected lots and is found to contain these impurities, it is recommended you discontinue use immediately and follow the outlined safety measures.
For further clarification, visit the **official recall announcement**: [Health Canada Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/sandoz-fesoterodine-fumarate-8-mg-tablet-out-specification-diester-impurity-0).
### What You Should Do
If you have purchased or are currently taking Sandoz Fesoterodine Fumarate 8 mg tablets, here are the next steps to ensure your safety:
- **Check your prescriptions**: Verify if your tablets are part of the affected lots. If so, stop using the product immediately.
- **Contact your healthcare provider**: Let your doctor or pharmacist know about the recall. They can guide you on alternative medications or prescribe replacements.
- **Return the product**: Take the affected medication to your pharmacy for proper disposal and inquire about any available refunds or replacements.
- **Report adverse effects**: If you’ve experienced any negative side effects while taking this medication, report them to Health Canada through their MedEffect system.
Taking prompt action is essential for managing your health and minimizing risks associated with this recall.
### Stay Safe – Get Instant Recall Alerts
Recalls like this highlight the importance of staying informed about potential health hazards. With so many medications and products in circulation, it can be daunting to keep up.
Simplify the process by downloading a reliable recall-tracking app. Get real-time alerts, easily verify your products, and stay ahead of critical safety updates. Protect yourself and your loved ones by staying informed!
Health is non-negotiable—act fast and stay aware. For official updates, visit [Health Canada Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/sandoz-fesoterodine-fumarate-8-mg-tablet-out-specification-diester-impurity-0).
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**Note to Readers**: This blog post is meant to keep you informed about current recalls impacting your safety. Always consult your healthcare provider with any concerns or questions regarding your medication.