# Major Recall Alert: Hemospray® Kit Recalled Due to Activation Knob Safety Issue
On November 4, 2024, an important recall was issued for certain lot numbers of the **Hemospray® Kit** due to a safety concern with nonconforming raw materials. The defect may cause the red activation knob to crack or break at its internal threading during use, which could result in the activation knob and carbon dioxide cartridge exiting the handle with potential force. This poses a serious risk for medical professionals and patients alike, making immediate action critical.
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## Why This Recall is Important
The safety of medical devices is paramount, especially when they are used in potentially life-saving procedures. In this case, the identified defect in the **Hemospray® Kit** could occur:
- **During activation** of the device
- **During use** in a medical procedure
- **After the procedure is completed**
Damage to the red activation knob could lead to accidental release of its components under pressure, posing risks of injury to both healthcare providers and patients. Additionally, any malfunction of this device during critical medical use could compromise care quality, causing further concerns for hospitals, clinics, and medical professionals who rely on its functionality.
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### Details of the Recall
Below are the key facts about the **Hemospray® Kit** recall:
- **Product impacted:** Hemospray® Kit
- **Brand Name:** Hemospray®
- **Reason for recall:** Certain devices were manufactured using nonconforming raw materials, which may cause the red activation knob to crack or break during or after use, leading to the possibility of carbon dioxide cartridge ejection.
- **Risks involved:** Risk of injury from forceful ejection, compromised device functionality, and potentially delayed medical care due to device failure.
- **Recall start date:** November 4, 2024
The recall affects only specific lot numbers. If you use or distribute the Hemospray® Kit, it is essential to review the lot numbers of all devices in your inventory and take corrective actions immediately.
For additional official details, visit the Canadian recall database [here](https://recalls-rappels.canada.ca/en/alert-recall/hemosprayr-kit).
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### What You Should Do
If you currently use or distribute Hemospray® Kits, follow these steps to stay safe:
1. **Check the affected lot numbers:** Review your inventory and identify if any of your Hemospray® Kits are part of the recall.
2. **Stop using recalled devices immediately:** Prevent further risk by discontinuing use of the defective devices.
3. **Contact the manufacturer or distributor:** Reach out to the supplier for instructions on returning the impacted products and obtaining replacements or refunds.
4. **Report concerns or incidents:** If any adverse events or problems have occurred with the Hemospray® devices, notify the appropriate regulatory authority and healthcare leadership immediately.
Ensuring the safety of medical staff and patients is critical. Take quick action to mitigate any potential hazards associated with this recall.
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## Stay Safe – Get Instant Recall Alerts
Recalls of medical devices like the **Hemospray® Kit** highlight the importance of staying updated on product safety issues. To protect patients and ensure compliance within your practice or organization:
- **Download a trusted recall alert app.** An app can provide real-time updates, customizable alerts, and instant notifications directly to your device.
- **Subscribe to official recall notifications:** Regularly check resources like the [Canadian Recall Database](https://recalls-rappels.canada.ca/en/alert-recall/hemosprayr-kit) for updates on similar safety announcements.
Be proactive about product safety and compliance. Download an alert app today and safeguard yourself, your workplace, and your patients against unforeseen risks.
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By taking swift action based on this recall notice, medical practices can prioritize safety and continue to deliver the highest quality of care. Stay informed, stay safe, and minimize risks to protect those who trust you with their health.