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Blueprint Mixed Reality Box Base, Blueprint Mixed Reality BP MXR Coracoid Cla...

# Major Recall Alert: Blueprint Mixed Reality Box Base, BP MXR Coracoid Clamp, Depth Stop Pin, Glenoid Digitizer, Glenoid Pin Guide, Instrument Check Block, and Glenoid Box Lid Recalled Due to Exceeded Complaint Rate Threshold

On **February 24, 2025**, a significant recall was issued for multiple components of the **Blueprint Mixed Reality Guidance Instrumentation System**. The recall affects the **Blueprint Mixed Reality Box Base**, **BP MXR Coracoid Clamp**, **BP MXR Depth Stop Pin**, **BP MXR Glenoid Digitizer**, **BP MXR Glenoid Pin Guide**, **BP MXR Instrument Check Block**, and the **Blueprint Mixed Reality Glenoid Box Lid**. The manufacturer identified a **nonconformance issue**, as the complaint rate related to operational difficulties exceeded the anticipated threshold.

This development raises safety concerns for medical professionals and patients, emphasizing the importance of addressing issues with this innovative surgical assistance system. Here's what you need to know about the recall and its implications.

## Why This Recall is Important

The **Blueprint Mixed Reality Guidance Instrumentation System** was designed as an innovative tool to improve surgical precision. However, complaints have surfaced regarding significant **user difficulties** during its operation. The overall complaint rate has now surpassed the acceptable limit, prompting the recall.

Why does this matter? Any equipment-related issues during surgical procedures can pose risks to patient safety and reduce the expected medical outcomes. By proactively addressing these challenges, the recall aims to prevent accidents, delays, or misuse during critical procedures.

This recall affects the following **Blueprint Mixed Reality** products:
- **Box Base**
- **BP MXR Coracoid Clamp**
- **BP MXR Depth Stop Pin**
- **BP MXR Glenoid Digitizer**
- **BP MXR Glenoid Pin Guide**
- **BP MXR Instrument Check Block**
- **Glenoid Box Lid**

If you're involved in using this instrumentation system or know a medical professional who relies on it, reviewing the recall instructions is crucial.

## Details of the Recall

The recall was initiated on **February 24, 2025**, after complaints regarding the **Blueprint Mixed Reality Guidance Instrumentation System** were thoroughly investigated.

### Affected Products
- **Brand:** Blueprint Mixed Reality
- **Specific Components:**
- Blueprint Mixed Reality Box Base
- BP MXR Coracoid Clamp
- BP MXR Depth Stop Pin
- BP MXR Glenoid Digitizer
- BP MXR Glenoid Pin Guide
- BP MXR Instrument Check Block
- Glenoid Box Lid

### Reason for Recall
The recall was issued due to **exceeded complaint rate thresholds related to difficulties in using the system**.

### Risks
If the issue is not addressed, continued use could compromise the intended performance of the system, leading to potential surgical delays or risks for patients.

For more details, visit the **official government recall listing**: [Click here](https://recalls-rappels.canada.ca/en/alert-recall/blueprint-mixed-reality-guidance-instrumentation-system).

## What You Should Do

If you own or use the affected components of the **Blueprint Mixed Reality Guidance Instrumentation System**, follow these steps:

1. **Stop using the affected products immediately** to ensure patient and operator safety.
2. **Contact the manufacturer** or distributor to initiate a return or replacement.
3. Check your inventory and quarantine all affected items to prevent unintended use.
4. Stay informed by registering for updates or contacting the official recall hotline for further guidance.

Medical facilities must also train their staff on handling recalls and assessing alternative solutions to maintain uninterrupted services.

## Stay Safe – Get Instant Recall Alerts

Product recalls can happen unexpectedly and impact critical industries, including healthcare. To stay ahead of recalls and ensure compliance, download the **MyRecalls App** today.

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- Instant notifications on recalls that matter to your industry.
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[Download the MyRecalls App now](https://myrecalls.app) and protect yourself from product risks every day.

## Final Thoughts

Recalls like this underscore the importance of maintaining high standards in medical device development and use. If you’re impacted by the **Blueprint Mixed Reality Guidance Instrumentation System recall**, act now to address the issue and ensure safety for all.

For further updates and official recall details, refer to the government’s resource: [Blueprint Mixed Reality Guidance Instrumentation System Recall](https://recalls-rappels.canada.ca/en/alert-recall/blueprint-mixed-reality-guidance-instrumentation-system).

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