# Major Recall Alert: ICU Medical Recalls Bag Spike, Clave, Chemolock, and Other Products Due to Manufacturing Issue with ChemoLock Ports
ICU Medical has issued an important recall affecting several critical medical devices, including Bag Spike, Clave, Chemolock, ChemoLock Admin Set, ChemoLock Bag Spike, ChemoLock Vial Spike, and more. The recall stems from a manufacturing defect impacting the weld of the ChemoLock port, which may cause the port to separate or break, leading to potential leaks during use. The affected products are essential in chemotherapy and medical infusion treatments, making this a serious issue for healthcare providers and patients alike.
If you use or distribute these products, here’s what you need to know.
## Why This Recall is Important
This recall addresses a specific manufacturing defect that compromises the functionality and safety of the ChemoLock port. ICU Medical discovered that the weld on certain lots of ChemoLock ports was not functioning as intended. This defect can lead to:
- **Port separation or breaking during use**
- **Fluid leaks that may pose health hazards**
The compromised weld can also create safety risks during medical procedures, particularly for chemotherapy patients, where the integrity of medical devices is crucial for delivering treatment safely.
## Details of the Recall
### Impacted Products:
The recall targets a range of medical devices used in chemotherapy and portable infusion systems. The affected product brands and types include:
- **Bag Spike**
- **Clave**
- **Chemolock**
- **ChemoLock Admin Set**
- **ChemoLock Bag Spike**
- **ChemoLock Vial Spike**
- **Ext Set W/ChemoLock**
- **Y Connector**
- **Rotating Luer**
- **Oncology Kit**
- **Transfer Set**
The recall specifically applies to lots that include the ChemoLock port. To verify if your products are affected, visit the official recall site at [Canada Recalls and Safety Alerts](https://recalls-rappels.canada.ca/en/alert-recall/chemolock-port).
### Recall Reason:
The manufacturing defect identified by ICU Medical compromises the weld in the ChemoLock port, potentially leading to:
- Separation during medical use
- Dangerous fluid leaks that can harm healthcare workers or patients
### Recall Announced on:
**October 23, 2023**
## What You Should Do
If you are in possession of the affected products, follow these steps to ensure the safety of your medical staff and patients:
1. **Isolate Affected Products**: Stop use immediately if you suspect you have products from the affected lot.
2. **Inspect Your Inventory**: Check the affected lot numbers as listed in the official recall notice [here](https://recalls-rappels.canada.ca/en/alert-recall/chemolock-port).
3. **Contact ICU Medical**: Notify ICU Medical for further instructions, including product return or replacement options.
4. **Alert Your Staff**: Inform your healthcare team about the potential risks, and transition to safe, unaffected alternatives if necessary.
5. **Seek Medical Guidance**: If fluid leaks occurred during use, consult a medical professional to assess any potential exposure risks.
Your proactive action in removing and returning these defective items can prevent harm and ensure continued patient safety.
## Stay Safe – Get Instant Recall Alerts
Keeping up with product recalls is crucial, especially when it involves life-saving medical devices like these. Instead of relying on sporadic updates, download our **free recall alert app** for instant notifications straight to your phone.
With our app, you can:
- **Receive real-time alerts on recalls in your region**
- **Search product safety databases**
- **Take action quickly to ensure safety**
[Click here to download the app now and stay informed.](#)
**Don’t Wait – Protect Your Patients and Staff Today.**
For more information on the recall, visit the official source: [Canada Recalls and Safety Alerts](https://recalls-rappels.canada.ca/en/alert-recall/chemolock-port).
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