# Major Recall Alert: Sysmex DI-60™ Main Unit Recalled Due to Risk of Incorrect Barcode Reading and Result Misattribution
Sysmex Corporation has issued an urgent recall for their **Sysmex DI-60™ Main Unit** due to a potential issue with barcode reading. When analyzing slides with unreadable barcodes, the device may inaccurately record or misattribute results. This problem is particularly prevalent with certain barcode scanners and specific barcode placements, increasing the risk for errors in diagnostic results. Interim measures have been advised, and a firmware upgrade is set to address the issue.
Stay informed about this critical recall to protect the integrity of your results and ensure operational safety.
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## Why This Recall Is Important
Accurate diagnostic results are the cornerstone of healthcare delivery, making it crucial for laboratory equipment to perform flawlessly. The **Sysmex DI-60™**, a vital unit for automating slide analysis, faces a serious functionality issue when dealing with unreadable barcodes. This problem could lead to:
- **Misattribution of results**, potentially affecting patient care.
- **Inaccurate diagnostic data**, jeopardizing clinical decisions.
- Increased **workload for labs**, as additional quality checks may be needed.
Sysmex has taken steps to address the issue by issuing guidance on interim measures and promising firmware upgrades to affected units. Staying updated on this recall is essential for users who rely on this equipment in critical medical and laboratory settings.
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## Details of the Recall
Here’s what you need to know:
- **Category**: Medical Equipment Recall – Canada (CAN)
- **Brand & Product**: Sysmex DI-60™ Main Unit
- **Issue**: Risk of incorrect barcode reading and misattribution of results when analyzing slides with unreadable barcodes.
- **Contributing Factors**: The issue is more likely with certain readers and barcode placements.
- **Safety Measures**:
- Follow interim instructions provided in the official notice.
- Await firmware upgrades, which will be provided for affected units to resolve the issue.
- **Date Announced**: October 16, 2023 (reference ID: 30385)
- **Image of Recalled Product**:
For the official recall notice, click [here](https://recalls-rappels.canada.ca/en/alert-recall/sysmex-di-60tm-main-unit).
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## What You Should Do
If you're using the Sysmex DI-60™ Main Unit in your facility, here are the immediate steps to take:
1. **Review the Recall Notice**: Carefully read the official guidance at the [recall page](https://recalls-rappels.canada.ca/en/alert-recall/sysmex-di-60tm-main-unit).
2. **Follow Interim Measures**: Sysmex has provided temporary solutions to minimize errors until the firmware upgrade is complete.
3. **Contact Sysmex Support**: Reach out to Sysmex’s customer service to confirm whether your unit is affected and for further assistance.
4. **Monitor Patient Results**: Increase quality control checks to avoid misattributions or inaccurate results.
By taking proactive measures, organizations can mitigate risks and ensure the safety and reliability of diagnostic operations.
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## Stay Safe – Get Instant Recall Alerts
Equipment recalls like this underscore the importance of staying updated to prevent operations from being disrupted or patient care compromised. Don’t miss any critical recalls in the future!
**Download the MyRecalls App today** to:
- Receive instant recall alerts.
- Track affected products in your inventory.
- Access critical safety updates in real time.
Stay informed, stay safe, and protect what matters most. [Download the app now!](#)
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By promptly responding to this recall and implementing Sysmex’s interim guidance, users can ensure uninterrupted, safe, and accurate diagnostic operations. For more information, visit the official [Sysmex recall page](https://recalls-rappels.canada.ca/en/alert-recall/sysmex-di-60tm-main-unit). Stay vigilant, and act now to address this issue.