# Major Recall Alert: BD Trucount™ Control Bead Kit, 30 Test, CE-IVD Recalled Due to Incorrect Labeling of Standard Deviation (SD) Values
On **July 8, 2025**, BD issued a critical recall for its **Trucount™ Control Bead Kit, 30 Test, CE-IVD**. An increasing number of complaints have surfaced regarding errors in the labeling of the standard deviation (SD) values for low and high control beads in the kit. These inaccuracies compromise the proper calculation of bead counts, potentially affecting test results and jeopardizing their reliability. Here’s everything you need to know about this **urgent product recall** and what steps to take if your practice uses this product.
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## Why This Recall is Important
The BD Trucount™ Control Bead Kit plays an essential role in diagnostic testing, offering precise calculations that ensure the accuracy of bead counts. However, the observed issue with misrepresented SD values on the product's labeling poses significant concerns:
- **Impact on Accurate Diagnostics**: Incorrect SD values could lead to false calculations, undermining the reliability of medical results.
- **Compromised Patient Care**: Faulty data could lead to delays, misdiagnoses, or improper treatment decisions.
- **Risk for Healthcare Providers**: Using mislabeled control bead kits could result in compliance issues and potentially harm a facility's reputation.
Due to the risks involved, healthcare professionals and facilities using these kits must take immediate action to ensure patient safety.
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## Details of the Recall
### Key Information:
- **Category**: Healthcare product recall (Canada)
- **Product Name**: **BD Trucount™ Control Bead Kit, 30 Test, CE-IVD**
- **Brand**: BD
- **Recall Start Date**: **July 8, 2025**
- **Reason for Recall**: Labeling errors in SD values for low and high control beads, which compromise the accuracy of bead count calculations.
- **Official Notification**: [Government of Canada Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/bd-trucounttm-control-bead-kit-30-test-ce-ivd)
This recall highlights BD’s increasing trend in complaints about the product, signaling the need for immediate corrective measures to avoid further complications.
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## What You Should Do
If your practice or facility uses the **BD Trucount™ Control Bead Kit**, here’s what you need to do:
1. **Stop Using the Product**: Immediately halt all use of affected kits to prevent any unreliable results.
2. **Check Your Inventory**: Identify whether your stock includes any of these recalled kits.
3. **Contact BD**: Reach out to BD’s customer service for guidance on returning or replacing affected products.
4. **Follow Official Instructions**: Refer to the official government recall notice for further steps on handling this product recall.
5. **Communicate with Your Team**: Inform your healthcare staff about the recall to ensure no further usage of the defective kits.
Acting swiftly can help ensure patient safety and protect your practice from potential issues related to compromised results.
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## Stay Safe – Get Instant Recall Alerts
Staying updated with recall news is essential for healthcare providers and consumers alike. Real-time alerts not only keep you informed but also help you take proactive action to minimize risks.
### Protect Your Health and Practice:
✅ **Download our free app today** to receive instant notifications about recalls like this one. With our app, you’ll stay ahead of critical product updates and ensure safety in your household or facility.
Don’t wait—**[Download the app now](#)** to safeguard yourself and your loved ones.
For more information about this recall, visit the official notice here: [BD Trucount™ Control Bead Kit Recall Alert](https://recalls-rappels.canada.ca/en/alert-recall/bd-trucounttm-control-bead-kit-30-test-ce-ivd).
Stay vigilant and take the necessary steps to ensure safety in your clinical environment today!