# Major Recall Alert: CADD-Solis VIP™ Ambulatory Infusion Pump and CADD-Solis™ Ambulatory Infusion Pump Recalled Due to Serious Battery-Related Issues
On **April 8, 2025**, the **CADD-Solis VIP™ Ambulatory Infusion Pump** and **CADD-Solis™ Ambulatory Infusion Pump** were officially recalled in Canada due to serious safety concerns related to their **battery packs** and **circuit boards**. This recall affects a critical medical device widely used in healthcare for delivering controlled infusions to patients. The issues involve **potential melting of the plastic housing** and **electrical shorts**, leading to potential safety hazards.
Let’s dive into the details of this recall and understand why prompt action is essential if you or a loved one relies on these devices.
## Why This Recall is Important
This recall addresses serious issues that could result in safety risks, including overheating, potential fires, or device malfunction. Healthcare providers and patients rely on these pumps for critical medication administration, making any flaw a potentially life-threatening concern. Below are the major reasons for the recall:
### Main Issues:
1. **Rechargeable Battery Circuit Board Damage**: Damage to the circuit board within the battery pack housing may result in **melting of the plastic housing** on both the top and bottom surfaces.
2. **Wireless Communication Module Circuit Board Damage**: Similar circuit board damage may cause **melting of the plastic housing** in the wireless communication module’s battery compartment.
3. **Battery Separator or Foreign Object Issues**: Damaged/dislodged battery separators or foreign materials inside the battery compartment may cause an **electrical short**, significantly increasing the risk of overheating.
Given that failure of these devices could jeopardize patient safety, it is imperative to address the recall immediately.
## Details of the Recall
**Brand**:
CADD-Solis VIP™ and CADD-Solis™ ambulatory infusion pumps.
**Issues Identified**:
- Potential melting of plastic housing from circuit board damage.
- Risk of electrical shorts caused by faulty battery separators or internal debris.
**Recall Date**:
April 8, 2025.
**Official Recall Source**:
For complete details, visit the [official government recall page](https://recalls-rappels.canada.ca/en/alert-recall/cadd-solistm-ambulatory-infusion-pump).
If you are a healthcare provider or a patient using these devices, take action now by following the outlined safety steps.
## What You Should Do
Healthcare professionals and individuals relying on these infusion pumps should take the following steps promptly:
- **Stop Using the Device**: If possible, discontinue using any affected CADD-Solis VIP™ or CADD-Solis™ pumps immediately.
- **Contact the Manufacturer**: Reach out to the manufacturer for further guidance on replacements or potential corrective actions.
- **Check Recall Notifications**: Monitor alerts from official channels or healthcare facilities to stay updated.
- **Inspect the Device**: Check for any signs of overheating such as warped plastic or a burning smell. Avoid charging or connecting power to any affected units.
By acting swiftly, you can help prevent risks and ensure continued patient safety.
## Stay Safe – Get Instant Recall Alerts
Don’t miss critical recall updates that may impact your health and safety. **Download our free recall alerts app today** and stay informed about the latest recalls on products you use every day. Be proactive, stay safe, and protect the ones you love.
For further information, please visit the **[official recall source here](https://recalls-rappels.canada.ca/en/alert-recall/cadd-solistm-ambulatory-infusion-pump).**
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By keeping informed and taking the necessary precautions, you can ensure the safety and well-being of your loved ones. Don’t wait—spread the word and share this important recall information with others!