# Major Recall Alert: Disposable Nasal Cannula Recalled Due to Partial Blockage Defect
If you depend on oxygen delivery systems, this is an important recall alert! The **Disposable Nasal Cannula R-1701S** has been recalled due to a possible defect that may prevent the reliable delivery of oxygen. A manufacturing issue could cause one side of the nasal passage opening to become partially blocked, which may impede proper oxygen flow to the user.
The recall, initiated by the manufacturer, comes after one customer registered a complaint about the defective nasal cannula. Fortunately, **no patient injuries or adverse health effects** have been reported as a result of this issue. The recall officially started on **March 3, 2025**.
Learn more about how this issue could affect you and what you can do to ensure your safety below.
## Why This Recall is Important
Oxygen delivery devices—like the **Disposable Nasal Cannula R-1701S**—are vital in ensuring that patients receive a steady and dependable flow of oxygen. Any defect, even a seemingly minor blockage, can have serious implications for users who depend on these devices for chronic conditions or medical treatment.
The **partial blockage defect** identified in the cannula could compromise the device's functionality, creating *a risk of insufficient oxygen delivery*. While no injuries have been reported so far, this recall is critical to prevent potential health risks for users. Oxygen therapy is not something you can take lightly, which makes staying informed a must for both patients and caretakers.
## Details of the Recall
Here’s what you need to know about the recall:
- **Category**: Medical Device – Disposable Nasal Cannula
- **Brand**: Disposable Nasal Cannula
- **Model Number**: R-1701S
- **Reason for Recall**: Partial blockage on one side of the nasal cannula could prevent oxygen from being delivered correctly.
- **Recall Start Date**: March 3, 2025
- **Known Incidents**: One customer complaint recorded, no reported injuries or harm to users.
This issue was identified after a customer complaint prompted a thorough review of the product, leading to the discovery of the potential defect. In response, the manufacturer has taken proactive steps to address the issue, including initiating the product recall to prevent any possibility of harm.
For additional official information, you can visit the recall announcement page here: [Government of Canada Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/disposable-nasal-cannula).
## What You Should Do
If you have purchased or are using a Disposable Nasal Cannula R-1701S, here are the recommended actions:
- **Stop Using the Product**: Immediately cease using any affected or potentially faulty nasal cannula to prevent risks from compromised oxygen delivery.
- **Contact the Manufacturer or Supplier**: Get in touch with the manufacturer or the point of sale for instructions on how to return the product and request a replacement or refund.
- **Consult a Healthcare Provider**: Speak to your healthcare provider to ensure you're continuing to receive adequate oxygen support while you transition to a replacement device.
Taking swift action can help mitigate risks and ensure your medical needs are met safely.
## Stay Safe – Get Instant Recall Alerts
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For the latest recall updates and guidance, check the official announcement at the Government of Canada’s recall page: [Disposable Nasal Cannula Recall](https://recalls-rappels.canada.ca/en/alert-recall/disposable-nasal-cannula).
Be proactive about your health—never miss an important safety alert again!