# Major Recall Alert: Burette Set (Clave, Shut-Off) Recalled Due to Tubing Separation Issue
ICU Medical has announced a critical recall for their **Burette Set (Clave, Shut-Off)** IV sets, citing a **lot-specific issue where the tubing connected to the burette component may separate due to insufficient solvent bonding**. This defect poses serious risks during medical procedures, making it essential for healthcare providers and institutions to take immediate action.
---
## Why This Recall is Important
Properly functioning medical devices are crucial for patient safety, particularly in settings where intravenous therapy is administered. The **Burette Set (Clave, Shut-Off)** IV sets in question have a known issue with tubing separation at the burette component. This problem arises from **insufficient solvent bonding** between the tubing and the burette, potentially disrupting therapy and risking harm to the patient.
This defect could lead to:
- **Interrupted IV flow** during critical treatments.
- **An increased risk of contamination** due to exposed connections.
- **Potential delays in emergency interventions**, which could have serious or even life-threatening consequences.
Healthcare providers who rely on this product should prioritize checking their inventory to ensure they are not using recalled lots. Immediate action can help prevent avoidable risks and ensure patient safety.
---
## Details of the Recall
Here are the key details of this recall for quick reference:
- **Category**: Medical Device (CAN)
- **Brand**: Burette Set (Clave, Shut-Off)
- **Affected Product**: Burette Set (Clave, Shut-Off) IV sets
- **Issue**: Tubing connected to the burette may separate due to insufficient solvent bonding.
- **Date Announced**: October 2023
- **Image of Product**: 
For more information regarding the recall, visit the **official source** [here](https://recalls-rappels.canada.ca/en/alert-recall/icu-medical-burette-set-clave-shut-0).
---
## What You Should Do
If you are a healthcare provider, facility manager, or caregiver using the **ICU Medical Burette Set (Clave, Shut-Off)**, follow these safety measures immediately:
1. **Check Inventory**: Identify and isolate the affected products from suspect lots. Refer to the official recall notice for specific lot numbers.
2. **Stop Usage**: Cease any further use of the recalled IV sets to prevent potential issues caused by tubing separation.
3. **Contact the Manufacturer**: Reach out to ICU Medical to initiate the return or replacement process. They should provide guidance on how to handle recalled products safely.
4. **Report Incidents**: If you’ve encountered problems related to this issue, report it to regulatory authorities like **Health Canada** to assist in monitoring the recall’s impact.
Act quickly to ensure safe and uninterrupted care for your patients. Enforcing these measures will help mitigate risks tied to this recall.
---
## Stay Safe – Get Instant Recall Alerts
Medical recalls like this are a serious reminder of how critical timely information is for maintaining safety. Stay ahead of product recalls affecting healthcare and everyday items by downloading the **MyRecalls App**.
- **Be the first to know** about new recalls.
- Access easy-to-read product descriptions and images.
- Get real-time alerts through your mobile device, ensuring you never miss urgent safety updates.
[**Download the MyRecalls App Now**](https://myrecalls.app) and protect your patients, family, and community today.
For more official details on this recall, visit the **Health Canada Recalls Page** [here](https://recalls-rappels.canada.ca/en/alert-recall/icu-medical-burette-set-clave-shut-0).
---
Ensure the **Burette Set (Clave, Shut-Off)** is removed from use immediately if affected. Prioritize safety by spreading the word about this recall and leveraging tools like the **MyRecalls App** for instant updates on future recalls. Keeping informed saves lives!