# Major Recall Alert: Epoc Blood Analysis Bgem Test Card and Epoc Blood Analysis System Recalled Due to Discrepant High pH Results
On March 25, 2025, Siemens Healthineers announced a major recall affecting the **Epoc Blood Analysis Bgem Test Card** and the **Epoc Blood Analysis System - Single Use Blood Gas, Electrolyte, and Metabolite Test Card** in Canada. The recall stems from **discrepant high pH results** caused by incorrect sample injection volumes when using specific software and sensor configurations. Read on to understand why this recall matters, what products are impacted, and what steps you should take to stay safe.
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## Why This Recall is Important
Accurate blood gas, electrolyte, and metabolite measurements are critical in clinical diagnostics for patient care. The problem identified with the **Epoc Blood Analysis Bgem Test Card** and **Epoc Blood Analysis System** could lead to **inaccurate pH readings**, which may delay or misdirect crucial medical treatments.
According to Siemens, the affected devices showed **discrepant high pH results** in samples injected beyond the **epoc reader beep** signal or after the **“analyzing sample”** message was displayed. This issue directly relates to the **sensor configuration 45.n**, which operates on specific software versions:
- **Epoc host v3.41.2**
- **Epoc nxs v4.14.9**
- **Epoc nxs v4.14.11**
These discrepancies could have serious clinical implications, especially in emergency or ICU settings where timely and accurate data is essential.
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## Details of the Recall
Here is an outline of the recall details:
- **Category**: Health and Medical Devices – Blood Analysis Tools
- **Brand**: Siemens Epoc
- **Affected Products**:
- **Epoc Blood Analysis Bgem Test Card**
- **Epoc Blood Analysis System - Single Use Blood Gas, Electrolyte, and Metabolite Test Card**
- **Issue**: Discrepant high pH results caused by higher injection volumes after the epoc reader beep or during the “analyzing sample” phase.
- **Sensor Configuration**: 45.n
- **Software Versions Impacted**:
- Epoc host v3.41.2
- Epoc nxs v4.14.9
- Epoc nxs v4.14.11
- **Recall Start Date**: March 25, 2025
To view the official recall notice, visit Canada’s government recall website [here](https://recalls-rappels.canada.ca/en/alert-recall/epoc-blood-analysis-bgem-test-card).
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## What You Should Do
If you’re using the affected **Epoc Blood Analysis** devices, take the following steps immediately to ensure patient and user safety:
1. **Stop using the affected products**: Discontinue use of any test cards or systems with the listed sensor configurations and software versions.
2. **Contact Siemens Healthineers**: Reach out to Siemens for further guidance on replacing or returning affected products.
3. **Review diagnostic procedures**: If discrepant pH results are suspected, consider reevaluating impacted test results and consult a healthcare professional if necessary.
4. **Alert your team**: Ensure all relevant personnel are informed of this recall and understand the risks associated with the affected products.
By taking these steps, you can minimize the risk of diagnostic errors and ensure the highest standards of patient care.
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## Stay Safe – Get Instant Recall Alerts
Recalls like this are a reminder of how important it is to stay informed. For immediate updates on recalls, download the **MyRecalls** app today! Our app helps you:
- Quickly identify recalled products you may be using.
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Don't compromise on safety. [Download the MyRecalls app now](https://myrecalls.app) and stay one step ahead of product safety issues.
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Staying proactive about medical device recalls can save lives. If you or your organization uses Siemens Epoc blood analysis systems, act immediately by following the steps outlined above. For official details on this recall, refer to the government recall notice [here](https://recalls-rappels.canada.ca/en/alert-recall/epoc-blood-analysis-bgem-test-card).
Stay safe, stay informed, and always prioritize patient care!