# Major Recall Alert: Endoflip System Recalled Due to Catheter Expiry Issue Post-2026
Attention healthcare professionals and medical facility managers: an important **recall alert** has been announced concerning the **Endoflip System**. The recall affects **EF and ES catheters** used with **EF-100 systems**, which will face a critical functionality issue starting **January 1, 2026**. This problem may result in catheters being incorrectly flagged as expired, rendering them unavailable for clinical procedures—a situation that could significantly impact patient care.
Read on for everything you need to know about this important recall, why it matters, and how to stay informed about future product safety issues.
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## Why This Recall is Important
The **Endoflip System** plays a crucial role in clinical procedures, and its proper functioning is vital for ensuring patient care. The recall focuses on a critical software issue involving the EF-100 system, specifically how it interacts with **EF and ES catheters** after **January 1, 2026**.
The problem arises from the system's **24-hour usage limit**, which will incorrectly flag these catheters as expired, making them unavailable for use. This software issue can lead to procedural delays, disruptions in medical workflows, and potential risks to patients requiring timely interventions.
For healthcare professionals relying on the Endoflip System for diagnostic or therapeutic procedures, this recall emphasizes a need for proactive solutions to address the defect ahead of the affected timeline.
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### Details of the Recall
Here’s a summary of the recall information:
- **Category**: Healthcare Equipment
- **Brand**: Endoflip System
- **Product**: EF and ES Catheters with EF-100 System
- **Issue**: The system's **24-hour usage limit** will incorrectly flag catheters as expired starting January 1, 2026, making them unavailable for clinical use.
- **Date Announced**: October 27, 2023
- **Safety Risks**: Procedural delays caused by unavailable catheters.
- **Image**:
- **Official Source**: [Endoflip Recall Notice on Recalls Canada](https://recalls-rappels.canada.ca/en/alert-recall/endoflip-system)
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### What You Should Do
If your healthcare facility uses the **Endoflip System**, it’s vital to take the following steps:
- **Identify Affected Products**: Confirm if your EF-100 systems use EF or ES catheters that could face this expiration flag issue after January 1, 2026.
- **Contact the Manufacturer**: Reach out to the system manufacturer to inquire about software updates, potential fixes, or guidance on avoiding disruptions.
- **Plan for Contingencies**: Establish backup protocols for affected procedures and ensure staff are trained to manage delays should the issue arise.
- **Report Issues**: If you encounter problems related to this defect before the recall update is implemented, report them promptly to the appropriate regulatory body.
Staying informed and prepared is the best way to minimize disruptions to care and ensure patient safety.
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### Stay Safe – Get Instant Recall Alerts
Product recalls can happen at any time, and staying on top of the latest updates is essential, especially in the healthcare sector. To ensure you never miss critical safety announcements like this, **download the [MyRecalls App](#)** today.
With the MyRecalls App, you’ll enjoy:
- Instant notifications on product recalls across multiple categories.
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- A user-friendly interface tailored to keep you informed.
**Download the app now** and safeguard your workplace, products, and patients.
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For more information on this recall, visit the official [Recalls Canada Alert](https://recalls-rappels.canada.ca/en/alert-recall/endoflip-system). Stay proactive and ensure your facility is well-prepared to handle these system challenges ahead of January 2026.