# Major Recall Alert: DiaStream Classic HD SNCO Recalled Due to Potential Particle in Venous Expansion Chamber
On **March 12, 2025**, a recall was issued for the **DiaStream Classic HD SNCO** product, a hemodialysis device, due to the rare possibility of a particle being present in the venous expansion chamber. The particle, which may consist of material from the filter inside the chamber, poses potential risks during medical treatments. If you're using this product or work in the healthcare sector, it’s crucial to understand the recall details and take immediate action.
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## Why This Recall is Important
Recalls involving medical devices like **DiaStream Classic HD SNCO** are significant because they directly impact patient safety. In this case, the presence of a foreign particle in the venous expansion chamber could compromise patient care and lead to potential complications. Such inconsistencies, though rare, raise critical concerns about product integrity and reliability.
The **venous expansion chamber** plays an essential role in hemodialysis devices, trapping air and preventing possible blockages during treatment. If particles are introduced into the system, they could put patients at risk by obstructing blood flow or increasing the chance of embolism. As medical devices are carefully regulated, addressing this issue promptly is vital to ensure healthcare providers maintain the highest standard of care.
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## Details of the Recall
The following information has been released about the recall of the **DiaStream Classic HD SNCO** product:
- **Category:** CAN
- **Brand Name:** DiaStream Classic HD SNCO
- **Product Name:** DiaStream Classic HD SNCO
- **Recall Start Date:** March 12, 2025
- **Reason for Recall:** There may be a rare occurrence of a particle in the venous expansion chamber. The particle comprises the material from the filter found inside the chamber.
- **Safety Hazard:** The presence of the particle could interfere with the dialysis process, potentially leading to health risks for patients.
For additional information regarding this recall, please refer to the **official Government of Canada recall notice** [here](https://recalls-rappels.canada.ca/en/alert-recall/diastream-classic-hd-snco).
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## What You Should Do
If you’re a healthcare provider or patient who uses the **DiaStream Classic HD SNCO**, follow these steps immediately:
- **Discontinue Use:** Stop using the product and alert your healthcare provider or facility as soon as possible.
- **Check Your Inventory:** Medical facilities should inspect their stock to identify and remove the affected units.
- **Contact the Manufacturer:** Reach out to the product's manufacturer for further instructions and potential product replacement.
- **Report Adverse Effects:** If any incidents or complications have occurred, report them to Health Canada or your local regulatory authority.
- **Monitor Updates:** Stay informed via official channels for any further announcements or safety guidelines.
By taking these steps promptly, healthcare professionals and patients can help mitigate any potential safety risks related to this recall.
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## Stay Safe – Get Instant Recall Alerts
In today’s fast-paced world, staying informed about recalls is more essential than ever, especially when it comes to life-saving medical devices. Ensure you’re always updated by downloading a **recall alert app** to receive real-time notifications about recalls and potential hazards.
Stay ahead of future recalls, protect your patients, and keep your loved ones safe by using digital tools designed to deliver timely updates!
For more details on this recall, visit the official Government of Canada recall notice here: [DiaStream Classic HD SNCO Recall](https://recalls-rappels.canada.ca/en/alert-recall/diastream-classic-hd-snco).
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*Act swiftly and help spread awareness about the **DiaStream Classic HD SNCO** recall to ensure patient safety remains a top priority.*