# Major Recall Alert: Alcon Issues Field Safety Action for Constellation® UltraVit® and HyperVit® Vitrectomy Probes
Alcon has announced a **voluntary medical device field safety corrective action** for specific models of its **Constellation® UltraVit® (10k)** and **HyperVit® (20k) vitrectomy probes**. The recall addresses a defect that could cause the probes to **unexpectedly fail to actuate and cut during use**, posing potential risks during eye surgery. With the safety of eye care professionals and patients in mind, Alcon is urging healthcare providers to review this notice carefully.
This recall affects **Constellation® System** products, including the **Total Plus Combined Procedure Pak**, **Constellation® Vision System Total Plus Vitrectomy Pak**, and **HyperVit® Bevel Vitrectomy Probe**. For affected devices and recommended courses of action, keep reading.
## Why This Recall is Important
Alcon initiated this corrective action out of an abundance of caution due to the **potential for increased safety risks to patients** during eye surgeries. The issue arises from possible probe malfunction, where the devices might **fail to actuate or cut as expected**.
### Potential Risks:
- If a probe unexpectedly fails during surgery, the position of the cutter and the amount of suction pressure applied could lead to:
- **Increased traction on the vitreous and/or retina.**
- Possibility of **holes, tears, or other damage to the retina.**
- **Adverse surgical outcomes** that could require further medical attention.
While the chances are remote, the severity of complications necessitates **proactive measures** to prevent risks during critical surgical procedures.
## Details of the Recall
The **voluntary field safety corrective action** specifically impacts select Alcon vitrectomy probe models. Below are the key details:
- **Recalled Products**:
- **Constellation® System**
- **Total Plus Combined Procedure Pak**
- **Constellation® Vision System Total Plus Vitrectomy Pak**
- **HyperVit® Bevel Vitrectomy Probe**
- **Probe, Posterior Vit**
- **Reason for Recall**:
The probes may unexpectedly **fail to actuate and cut during use**, creating potential surgical risks.
- **Potential Impact**:
Retinal holes or tears caused by excess traction during surgeries if the probe malfunctions.
For specific product codes or additional details, visit the [official recall page](https://recalls-rappels.canada.ca/en/alert-recall/constellationr-ultravitr-and-hypervitr-vitrectomy-probe).
## What You Should Do
If you are a healthcare provider or facility using any of the affected devices, follow these **necessary steps**:
- **Cease Use Immediately**: Discontinue use of affected products listed in Alcon's recall notice to avoid potential surgical complications.
- **Contact Alcon**: Reach out to the manufacturer for further guidance, including how to inspect devices, request replacements, or learn additional safety measures.
- **Inform Patients**: If you’ve used these probes in recent procedures, monitor patients carefully for any signs of complications, such as retinal tears, to ensure prompt intervention if needed.
Alcon recognizes the importance of patient safety and is working closely with healthcare providers to minimize risks associated with the recall.
## Stay Safe – Get Instant Recall Alerts
Recalls like this emphasize the need to stay informed about medical device safety for both professionals and consumers. **Missing important recall information could have serious consequences.**
Download the free **MyRecalls App** today to receive **real-time updates on recalls for medical devices, food, medications, and more**. With instant notifications and detailed guidance, you’ll be equipped to act quickly when safety alerts arise.
Stay ahead of product safety updates and protect what matters most. For full details on this recall, visit the [official government recall notice](https://recalls-rappels.canada.ca/en/alert-recall/constellationr-ultravitr-and-hypervitr-vitrectomy-probe).
By staying informed, you help ensure the safety of your patients and maintain the highest level of care. Take action today!