# Major Recall Alert: Bard Dynamic Deca Steerable Diagnostic EP Catheter, Daig Livewire Steerable Diagnostic EP Catheter Recalled Due to Breached Sterile Barriers
Stryker Sustainability Solutions (SSS) has announced a recall involving **Bard Dynamic Deca Steerable Diagnostic EP Catheter** and **Daig Livewire Steerable Diagnostic EP Catheter**. Concerns have been raised about breaches in the sterile barrier on the chevron seal side of the primary Tyvek pouch, posing a risk to patient safety. This recall highlights the significance of fielding medical devices that meet rigorous quality standards, particularly for lifesaving tools like EP catheters.
## Why This Recall is Important
When it comes to medical devices, maintaining sterility is paramount for preventing infections during procedures. The breached sterile barriers reported in these catheters pose significant risks, including:
- **Compromised Sterility**: A breach in the sterile pouch could lead to contamination.
- **Potential Infections**: Devices contaminated with harmful microorganisms could cause severe infections in patients.
- **Safety Concerns During Use**: Physicians rely on the sterility of diagnostic EP catheters to ensure successful outcomes in cardiac procedures.
The health and safety of patients undergoing diagnostic and therapeutic procedures with these devices are directly at stake, making this recall an urgent matter for healthcare providers and facilities.
## Details of the Recall
Below are key details relating to this important recall:
- **Category**: Medical Device – Recalls and Safety Alerts in Canada
- **Affected Devices**:
- Bard Dynamic Deca Steerable Diagnostic EP Catheter
- Daig Livewire Steerable Diagnostic EP Catheter
- **Brand**: Bard and Daig, distributed by Stryker Sustainability Solutions (SSS)
- **Reason for Recall**: Breached sterile barriers on the chevron seal side of the primary Tyvek pouch, which may compromise sterility.
- **Date Announced**: This recall was announced on **October 19, 2023**.
- **Source**: For complete details, visit the official recall notice here: [Government of Canada Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/bard-dynamic-deca-steerable-diagnostic-ep-catheter-and-daig-livewire-steerable).
## What You Should Do
If you or your healthcare facility uses Bard or Daig steerable diagnostic EP catheters, follow these steps immediately:
1. **Stop Using the Affected Products**: Identify and quarantine all recalled devices to prevent further use.
2. **Notify Your Facility**: Inform your quality control team or department head about the recall.
3. **Contact Your Supplier**: Reach out to Stryker Sustainability Solutions (SSS) for instructions on returns, exchanges, or additional updates.
4. **Monitor Patients**: If the device has already been used, closely monitor patients for any signs of infection or complications.
5. **File a Report**: Report any adverse events or issues related to the use of these products to Health Canada.
Taking swift action is crucial to safeguard patients and maintain safe clinical practices.
## Stay Safe – Get Instant Recall Alerts
Recalls like this highlight the importance of staying informed about product issues that could impact patient safety. To ensure you never miss critical updates:
- **Download an App for Alerts**: Stay ahead of recalls by downloading a trusted recall alert app. This will enable you to receive instant alerts on essential products, including medical devices, food, and more.
Patient safety should always be a top priority. By acting on recall notices promptly and following the recommended steps, we can help maintain the highest standards in healthcare.
For further details, access the official source: [Click here for the full recall notice](https://recalls-rappels.canada.ca/en/alert-recall/bard-dynamic-deca-steerable-diagnostic-ep-catheter-and-daig-livewire-steerable).
Stay informed, stay safe, and take prompt action to address this important issue!