# Major Recall Alert: LikoScale™ Adapter Kits and Q-LINK 13 Components Recalled Due to False Latching Hazard
Baxter Corporation has issued an **urgent medical device recall** for the **Q-LINK 13 lift component** and **LikoScale™ Adapter Kits** due to reports of potential hazards involving improper attachment (known as false latching) with the quick-release hook. This recall, initiated on **May 29, 2025**, addresses critical safety concerns. Read on for everything you need to know about this recall and the steps you should take.
Stay informed and protect yourself—**don’t miss these essential updates.**
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## Why This Recall is Important
Medical device safety is crucial, especially when it involves lifting components that play a vital role in caregiving and patient support. Baxter Corporation’s **Q-LINK 13 lift component**, included in the **LikoScale™ Adapter Kits**, has been flagged for a **false latching issue**. Improper attachment of the Q-LINK 13 quick-release hook can pose severe risks, including:
- **Accidental detachment** during use
- **Injury to patients and caregivers**
- **Malfunction during critical transfers**
These risks highlight why it’s vital to address this recall immediately to ensure the safety and proper function of medical equipment.
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### Details of the Recall
Here’s a quick breakdown of the key information regarding this urgent recall:
- **Brand Involved**: LikoScale™ Adapter Kits and Q-LINK 13 Components
- **Recall Date Initiated**: May 29, 2025
- **Reason for Recall**: Reports of improper attachment (false latching) with the quick-release hook, which can lead to serious safety concerns.
- **Affected Products**:
- **Q-LINK 13 Lift Component**
- **LikoScale™ Adapter Kits**, which contain the affected Q-LINK 13 component.
For detailed recall information, visit the **official source**: [Government of Canada Recall Alert – Q-LINK 13 Components and LikoScale™ Adapter Kits](https://recalls-rappels.canada.ca/en/alert-recall/q-link-13-components-and-likoscaletm-adapter-kits).
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### What You Should Do
If you or your organization uses any of the affected products, take the following actions immediately:
1. **Stop Using the Affected Products**: Discontinue using the Q-LINK 13 lift component and LikoScale™ Adapter Kits until further notice.
2. **Check Your Inventory**: Identify whether your equipment contains the Q-LINK 13 or LikoScale™ Adapter Kits with the quick-release hook.
3. **Contact the Manufacturer**: Reach out to Baxter Corporation for further instructions on product returns, replacements, or repairs.
4. **Report Suspected Incidents**: If you have experienced issues with the affected products, report them to Health Canada’s health products safety services.
Prompt action is critical to avoid potential injuries or hazards linked to this recall.
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### Stay Safe – Get Instant Recall Alerts
Safety recalls like this one highlight the importance of staying informed about the products you use every day. To ensure you never miss critical updates:
- **Download Recall Alert Apps**: These apps provide instant notifications for product recalls and safety alerts in your region.
- **Subscribe to Official Alerts**: Sign up for Health Canada’s email alerts to stay ahead of potential hazards.
Stay proactive to protect yourself, your patients, and your loved ones. Don’t wait—[click here](https://recalls-rappels.canada.ca/en/alert-recall/q-link-13-components-and-likoscaletm-adapter-kits) for the latest official updates on this recall.
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Baxter Corporation is committed to resolving this issue and ensuring the safety of their customers. As a user, your diligence in responding to recalls is a key step in maintaining both personal and public safety.
Stay informed, stay safe, and always act quickly when a recall is announced!