# Major Recall Alert: Equinoxe® Reverse Shoulder System - Humeral Liner Recalled Due to Manufacturing Non-Conformance
Exactech has issued an important recall of its **Equinoxe® Reverse Shoulder System - Humeral Liners** due to a critical manufacturing issue discovered at its Sarasota facility. This issue involved the spherical articular surface of the liners being positioned outside the standard tolerances specified in the engineering design. The recall, which officially began on **August 15, 2025**, could have significant implications for patients relying on these implants for joint stability and alignment.
If you or someone you know has received a shoulder implant using the Equinoxe® system, it’s vital to understand the details of this recall and what steps you should take next.
## Why This Recall is Important
The **Equinoxe® Reverse Shoulder System - Humeral Liners** play a crucial role in maintaining proper joint alignment and implant performance for individuals who have undergone shoulder replacement surgeries. Discovering that some liners have a **spherical articular surface positioned out of specification** raises serious concerns about:
- **Joint Misalignment**: Improper positioning may lead to discomfort, reduced range of motion, and complications with the implant's performance.
- **Implant Durability**: Non-conforming products may wear down faster than expected, requiring premature revision surgery.
- **Patient Safety**: Adverse outcomes could include joint instability, pain, or the inability to achieve proper shoulder motion.
Patients and medical professionals must act promptly to address this issue and ensure the safety of individuals relying on the Equinoxe® system.
## Details of the Recall
Here’s what you need to know about the **Exactech Equinoxe® Humeral Liner recall**:
- **Product Affected**: Equinoxe® Reverse Shoulder System - Humeral Liner
- **Brand**: Equinoxe®
- **Recall Reason**: Non-conformance of the spherical articular surface position discovered during inspection at Exactech's Sarasota facility.
- **Key Concern**: The surface positioning defect could affect joint alignment and implant functionality.
- **Recall Start Date**: August 15, 2025
- **Source Information**: Visit this official [Government of Canada recall page](https://recalls-rappels.canada.ca/en/alert-recall/equinoxer-reverse-shoulder-system-humeral-liner) for more details.
Exactech has emphasized the importance of addressing this concern promptly to mitigate risks to patients.
## What You Should Do
If you have an Equinoxe® Reverse Shoulder System implant or suspect that you may be affected by this recall, consider taking these steps:
- **Contact Your Healthcare Provider**: Reach out to your orthopedic surgeon or healthcare provider to discuss potential risks associated with your implant.
- **Monitor for Symptoms**: Watch for any unusual symptoms such as increased pain, reduced range of motion, or joint instability. Report these symptoms immediately to a medical professional.
- **Reach Out to Exactech**: For additional guidance, affected individuals should contact Exactech directly for further assistance on next steps.
- **Stay Up-to-Date**: Follow reputable sources like the [Government of Canada recall website](https://recalls-rappels.canada.ca/en/alert-recall/equinoxer-reverse-shoulder-system-humeral-liner) for updates on this recall and other important safety announcements.
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