# Major Recall Alert: Cardiac Electrophysiology (EP) Packs Recalled Due to Potential Syringe Defect in Medline Components
Cardinal Health has announced a critical **medical device recall** involving Cardiac Electrophysiology (EP) Packs, which may contain faulty components from Medline Industries. The recall specifically references issues with the **Namic Angiographic Control Syringes**, which pose a safety risk. A faulty syringe rotating adaptor may become loose or fully disconnect during use, leading to serious outcomes, especially in critical cardiac procedures. This article outlines everything you need to know about this recall, how it might impact you, and the steps you can take to stay safe.
## Why This Recall is Important
When it comes to medical procedures, the reliability of equipment is a non-negotiable factor. The Cardiac Electrophysiology (EP) Packs containing **Medline’s Namic Angiographic Control Syringes** have been recalled due to a significant issue: the rotating adaptor of the syringe may unwind during use.
This defect can result in:
- **Loose connections** between the syringe and manifold.
- **Full disconnections**, disrupting the functionality of the device.
Both scenarios pose risks during cardiac procedures, potentially delaying treatment and increasing the danger to patients. Cardinal Health’s proactive investigation has uncovered that some **Presource kits** shipped to customers included the affected Medline components, underscoring the importance of this recall.
Medical devices must ensure peak performance, particularly in life-or-death situations such as cardiac electrophysiology procedures. Even a minor flaw in equipment could have drastic consequences.
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## Details of the Recall
Affected brands and products:
- **Brand**: Cardinal Health
- **Product Name**: Cardiac Electrophysiology (EP) Packs
- **Primary Concern**: Namic Angiographic Control Syringes manufactured by Medline Industries.
Key recall issue:
- Defect: Rotating adaptor of the syringe may **unwind**, resulting in loose or disconnected joints between the syringe and manifold during use.
Key safety concerns:
- This design flaw could compromise the functionality of the syringe, affecting patient safety during critical heart procedures.
**Date Announced**: [31753]
For more official details, please refer to the official Government of Canada recall notice here: [Cardinal Health Cardiac Electrophysiology (EP) Packs Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/cardinal-health-cardiac-electrophysiology-ep-packs).
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## What You Should Do
If you work in healthcare or are responsible for medical devices, here are the steps you need to follow:
1. **Check Inventory**: Verify if you have any **Cardiac Electrophysiology (EP) Packs** in stock.
2. **Review Lot Numbers**: Refer to the detailed list of affected batch numbers from Cardinal Health or contact their customer service team for assistance.
3. **Quarantine Affected Products**: Immediately remove any identified products from your inventory to avoid accidental use.
4. **Contact Cardinal Health**: Notify the company for further instructions on returning or disposing of recalled products.
5. **Patient Safety**: Ensure that any procedures involving the affected components are rescheduled using alternative equipment to protect patient outcomes.
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## Stay Safe – Get Instant Recall Alerts
Protecting patient safety starts with staying informed. Recalls like this one highlight the importance of having immediate access to the latest product safety alerts. Be proactive – download an app or tool that provides instant notifications on recalls critical to your industry.
Our top recommendation? Track and manage recalls effortlessly through comprehensive recall tracking resources.
**Stay Updated, Stay Safe**: Keep your patients and team safe by monitoring product recalls in real-time. [Read the official recall details here](https://recalls-rappels.canada.ca/en/alert-recall/cardinal-health-cardiac-electrophysiology-ep-packs) for further updates.
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Faulty medical components can pose a significant risk, but informed actions can mitigate potential harm. Check your inventory, stay vigilant, and always respond promptly to recall alerts to ensure patient safety remains your top priority.