# Major Recall Alert: Inlay Optima™ Ureteral Stent Without Guidewire Kit, Length 30cm, 6Fr Recalled Due to Labeling Discrepancy
## Why This Recall is Important
BD has announced a significant recall of its **Inlay Optima™ Ureteral Stent Without Guidewire Kit, Length 30cm, 6Fr** following reports of a critical labeling issue. According to customer complaints, the **pouch label may not match the actual product within the packaging**, which can result in incorrect product use during medical procedures. As these stents are utilized for urinary drainage in patients with obstructions, accurate labeling is vital for safe and effective treatment.
Labeling discrepancies pose a potential risk to patient safety by increasing the likelihood of procedural errors. Healthcare professionals and organizations that use or distribute this product must take immediate action to address this recall.
## Details of the Recall
Here’s what you need to know about this important recall:
- **Brand Name**: Inlay Optima™
- **Product Name**: Inlay Optima™ Ureteral Stent Without Guidewire Kit, Length 30cm, 6Fr
- **Reason for Recall**: The pouch label does not consistently match the actual product, as determined by an internal investigation after customer complaints.
- **Category**: CAN (Canada)
- **Date Announced**: October 6, 2023
- **Source**: Health Canada
The **Inlay Optima™ Ureteral Stent Without Guidewire Kit** plays a crucial role in managing urinary blockages in patients. However, improper labeling can lead to healthcare professionals unknowingly using the wrong product, resulting in patient risk during medical procedures.
Healthcare facilities, distributors, and other stakeholders should discontinue the use of any affected products immediately and verify their inventory for compliance. To view the **official recall announcement** for more detailed information, visit the [official Health Canada recall page](https://recalls-rappels.canada.ca/en/alert-recall/inlay-optimatm-ureteral-stent-without-guidewire-kit-length-30cm-6fr).
## What You Should Do
If you or your healthcare organization has purchased this product, it’s essential to take the following steps to minimize risks:
- **Stop using affected products**: Inspect your inventory for any Inlay Optima™ Ureteral Stent kits. If you possess any of the affected products, immediately cease their usage.
- **Notify your team**: Inform your healthcare teams and staff about the recall and labeling discrepancy to avoid accidental use.
- **Contact BD for guidance**: Reach out to BD for further instructions on how to handle affected inventory and to inquire about replacement products or refunds.
- **Monitor patient safety**: If the product has already been used, ensure you monitor patient outcomes and report any adverse effects to the appropriate regulatory authorities.
- **Spread awareness**: Share recall details with your colleagues and relevant medical organizations to prevent potential risks.
For personalized advice or to ensure compliance, consult your healthcare provider or a professional distributor. Prompt action is necessary to safeguard patients and streamline corrective measures.
## Stay Safe – Get Instant Recall Alerts
Healthcare recalls like this highlight the importance of staying informed in real time. To ensure you are always updated on critical product recalls, consider downloading recall alert apps to get instant notifications directly to your smartphone.
By acting quickly, you can prevent potential mishaps and safeguard your practice. For full details regarding this recall, visit Health Canada’s official website [here](https://recalls-rappels.canada.ca/en/alert-recall/inlay-optimatm-ureteral-stent-without-guidewire-kit-length-30cm-6fr). Stay vigilant and take the necessary steps to keep your patients safe!
**Protect your patients. Stay informed. Download a recall alert app today!**