# Major Recall Alert: CellMek SPS Recalled Due to Volumetric and Handling Errors – Key Safety Alert
On **August 27, 2025**, a major product recall was issued for the **CellMek SPS** under critical conditions affecting its accuracy and performance. The recall addresses two pivotal issues:
1. The **dead volume discrepancies**, where the actual liquid retention values for **cassette B** (1582μl) and **cassette E** (2093μl) greatly exceed the stated volumes in the instructions for use (750μl and 1300μl, respectively).
2. Functional inaccuracy due to **cassette type E not being rocked** prior to aspirating the specimen, potentially compromising test results.
This recall is crucial for ensuring safety and reliability when using this advanced system. If you own or operate a **CellMek SPS**, it’s vital to be informed and take action.
To access the official recall notification, [click here](https://recalls-rappels.canada.ca/en/alert-recall/cellmek-sps).
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## Why This Recall is Important
Laboratory equipment like the **CellMek SPS** requires precise functionality to deliver reliable results, especially in critical clinical and diagnostic applications. The **dead volume discrepancies** and improper specimen handling in the **cassette module** can lead to:
- **Compromised accuracy** in diagnostic outcomes
- **Wasted specimens or reagents**, increasing operational costs
- **Delayed or false results**, impacting patient care and treatment plans
These issues pose significant risks in medical settings, highlighting the urgency of the recall.
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### Details of the Recall
The recall specifically addresses the following concerns:
- **Dead Volume Errors in Cassettes B & E**
- Stated dead volume for **cassette B**: 750μl (actual volume: 1582μl)
- Stated dead volume for **cassette E**: 1300μl (actual volume: 2093μl)
- Impact: Incorrect volumes could affect reagent usage, mixing ratios, and outcomes.
- **Handling Issue in Cassette Type E**
- Cassette type E is **not rocked** prior to aspirating the specimen as required.
- Impact: Could result in improper sample preparation, affecting test accuracy.
> **Brand**: CellMek SPS
> **Product**: CellMek SPS
> **Recall Start Date**: August 27, 2025
> **Official Source**: [Government of Canada Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/cellmek-sps)
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### What You Should Do
If you are using the **CellMek SPS**, follow these steps to address the recall:
- **Immediately stop using the affected product** to prevent compromised results.
- Review the current settings and instructions for use in comparison to the recall details.
- Contact the manufacturer for updated product guidelines and corrective measures.
- Report any adverse events related to this issue to the appropriate safety authority in your region.
For additional assistance, consult the official recall notice linked in the details section above or reach out to the product distributor or supplier.
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**Conclusion**
The recall of the **CellMek SPS** due to its volumetric and handling inaccuracies underscores the critical need for operational precision in advanced laboratory equipment. Addressing these issues promptly will safeguard against inaccuracies and inefficiencies. Stay informed, act swiftly, and adopt a proactive approach to recalls.
For full details on this recall, access the official source [here](https://recalls-rappels.canada.ca/en/alert-recall/cellmek-sps).