# Major Recall Alert: IceSeed 1.5 CX 90 Needle Recalled Due to Programming Issue
Boston Scientific has recently issued an advisory regarding its **IceSeed 1.5 CX 90 Needle**, an essential medical device widely used in healthcare. Needles manufactured between **April 2024 and February 2025** have been discovered to contain a critical programming error. Instead of operating under **commercial settings**, these devices were mistakenly set to **demo mode**, potentially leading to compromised device functionality.
The recall officially begins on **March 24, 2025**, according to a statement released by the company. If you're in the healthcare industry or use the IceSeed CX needle, here’s what you need to know.
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## Why This Recall is Important
Any medical device malfunction raises significant concerns about **patient safety** and **treatment outcomes**. These incorrectly programmed **IceSeed 1.5 CX 90 Needles** may impact their intended usage in medical procedures, posing a potential risk to patients. The switch to demo settings means the device will behave differently than expected under commercial conditions, which may affect the efficacy of medical procedures that rely on its performance.
By addressing this issue promptly and spreading awareness, Boston Scientific aims to mitigate risks and ensure healthcare professionals have the accurate tools they need to perform critical treatments successfully.
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## Details of the Recall
Here are the most important details to know about this recall:
- **Product Name**: IceSeed 1.5 CX 90 Needle
- **Brand**: Boston Scientific
- **Issue**: Needles manufactured between **April 2024 and February 2025** were programmed with demo settings instead of commercial settings.
- **Recall Start Date**: March 24, 2025
- **Safety Advisory Announced On**: March 24, 2025
- **Images of Recalled Product**:
- **Official Source of Recall Information**: [Government of Canada Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/iceseed-15-cx-90-needle)
Boston Scientific has notified customers about the advisory and is actively working to address the programming issue.
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## What You Should Do
If you currently use or manage medical devices in your facility, follow these steps to ensure compliance and safety:
1. **Check Your Inventory**: Identify whether any IceSeed 1.5 CX 90 Needles in your possession were produced between **April 2024 and February 2025**.
2. **Stop Usage Immediately**: If you find affected devices, stop using them right away to avoid complications in procedures.
3. **Contact Boston Scientific**: Reach out to the manufacturer to obtain further instructions on how to replace or reprogram the faulty devices.
4. **Retain Documentation**: Keep records of product serial numbers, purchase dates, and correspondence with the company for evidence of compliance.
Swift action is crucial to avoid any risks associated with this recall and to ensure patient safety.
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## Stay Safe – Get Instant Recall Alerts
Staying informed about recalls like this is essential for safety and compliance, especially when it comes to critical medical devices. Don’t miss potential recall notices in the future—download the **MyRecalls app** today for **real-time updates** on recalls in Canada and beyond.
With the app, you can:
- Get instant notifications about recalls for medical devices, food, vehicles, and more.
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[Download the MyRecalls App Now](#) to stay ahead and safeguard your health and safety.
For further information about the IceSeed 1.5 CX 90 Needle recall, visit the official Canadian recall notice on the [Government of Canada Recall Website](https://recalls-rappels.canada.ca/en/alert-recall/iceseed-15-cx-90-needle). Always be proactive in addressing recalls to keep safety a top priority.
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By acting immediately, you can help reduce risks and ensure the highest standards of health and medical safety are maintained!