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Apo-Dustasteride 0.5 mg Recall Due to Affected lot may contain undersized cap...

# Major Recall Alert: Apo-Dustasteride 0.5 mg Recalled Due to Undersized Capsules

Are you using Apo-Dustasteride 0.5 mg by APOTEX? A recent recall has been issued concerning a specific lot of this medication that may contain undersized capsules. Such discrepancies could impact the dosage consistency and effectiveness of the product, posing potential risks to users. Here's what you need to know about this recall, why it matters, and how to stay informed.

## Why This Recall is Important

Medical recalls are issued to protect consumers from potential health risks associated with defective or unsafe products. In this case, the recall of Apo-Dustasteride 0.5 mg was issued due to an affected lot containing undersized capsules. Undersized capsules may not deliver the prescribed amount of the medication, potentially lowering its effectiveness or disrupting the treatment regimen for individuals managing specific health conditions.

If you're affected by this recall, taking prompt action is crucial to ensure your safety. Read on for the full details.

## Details of the Recall

Here are the key details regarding the Apo-Dustasteride recall:

- **Product Name**: Apo-Dustasteride
- **Dosage**: 0.5 mg
- **Brand**: APOTEX
- **Category**: Pharmaceuticals
- **Reason for Recall**: The affected lot may contain undersized capsules, potentially impacting dosage accuracy.
- **Image of Product**:
![Apo-Dustasteride Product Image](https://myrecalls.app/images/products/29286_1752195808.jpg)
- **Date Announced**: October 2023
- **Source**: For more information, visit the official recall notice [here](https://recalls-rappels.canada.ca/en/alert-recall/apo-dustasteride-05-mg-affected-lot-may-contain-undersized-capsules).

This recall is part of ongoing safety measures intended to protect consumers from potential health risks associated with incorrectly manufactured medicinal products.

## What You Should Do

If you currently use Apo-Dustasteride 0.5 mg, here’s what you need to do to ensure your safety:

- **Check Your Medication**: Look at the packaging to determine if your medication is part of the recalled lot. If unsure, consult with your pharmacy.
- **Stop Using the Recalled Product**: If your medication is affected, discontinue use immediately.
- **Contact APOTEX or Your Pharmacy**: For guidance on next steps, including how to return the medication or obtain a replacement.
- **Consult Your Healthcare Provider**: If you’ve been using the affected medication, speak with your doctor to discuss any potential health effects or to explore alternative treatments.

Acting promptly is key to minimizing any potential risks associated with this recall.

## Stay Safe – Get Instant Recall Alerts

Recalls like this underscore the importance of staying informed about product safety. To ensure you never miss critical alerts on food, medications, and other consumer products, download the [MyRecalls App](https://myrecalls.app) today. With real-time notifications, you’ll always be informed about potential risks and the steps to take in response to recalls.

### Why Download MyRecalls?

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- Stay one step ahead in protecting your health and safety.

Don’t wait—stay proactive about your safety. Download the [MyRecalls App](https://myrecalls.app) now to stay alert and make informed decisions.

Protecting yourself and your loved ones from the risks associated with defective products starts with being in the know. For the full recall details on Apo-Dustasteride 0.5 mg, visit the [official recall notice here](https://recalls-rappels.canada.ca/en/alert-recall/apo-dustasteride-05-mg-affected-lot-may-contain-undersized-capsules). Stay informed, stay safe!

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