# Major Recall Alert: Omnipod Alternate Controller Insulin Pumps Recalled Due to Inner Tubing Tear Risk
The Omnipod® 5 Alternate Controller Enabled Insulin Infusion Pump has been voluntarily recalled by Insulet Corporation due to a potential manufacturing defect. Specific lots of Omnipod® 5 Pods may contain a small tear in the internal tubing that delivers insulin. This defect could result in insulin leaking within the Pod, preventing the proper infusion of medication into the body. If not addressed, the issue could lead to elevated blood glucose levels, increasing the risk of diabetic ketoacidosis (DKA).
Here is everything you need to know about this urgent recall, as well as steps to ensure your continued safety.
## Why This Recall is Important
The Omnipod® 5 system is designed to simplify diabetes management by delivering insulin efficiently and reliably. However, Insulet has identified a defect in the internal tubing of certain Pods from specific lots. This defect prevents insulin from reaching the body in adequate quantities and instead allows it to leak inside the Pod.
*Why this matters*:
- **Health Risks**: Insufficient insulin delivery may cause blood glucose levels to rise dangerously high, potentially resulting in diabetic ketoacidosis (DKA).
- **Reports of Adverse Events**: Eighteen adverse events, including hospitalizations related to elevated blood sugar, have been reported. Thankfully, no fatalities have occurred.
Insulet's swift action to identify and address the affected lots underscores its commitment to patient safety.
## Details of the Recall
Here are the key details users need to know:
- **Reason for Recall**: A small tear in the internal tubing of certain Omnipod® 5 Pods could cause insulin to leak inside the device. High blood glucose levels and, in severe cases, diabetic ketoacidosis (DKA) may result if proper insulin infusion is not achieved.
- **Products Affected**: Specific lots of Omnipod® 5 Pods distributed within the United States. All other Omnipod® products, including Omnipod® 5 Pods outside the identified lots, remain safe to use.
- **Customer Impact**: This issue impacts approximately 1.5% of global Omnipod® 5 Pod production, and Insulet has already updated its manufacturing process and quality controls to prevent further defects.
For additional details, visit the FDA’s official recall notice [here](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/insulet-initiates-voluntary-medical-device-correction-certain-omnipodr-5-pods-us).
## What You Should Do
If you are an Omnipod® 5 user, follow these steps immediately to confirm if your Pods are affected:
1. **Check Your Pods**: Visit [omnipod.com/check-pods](https://omnipod.com/check-pods) and enter your Pod lot number to confirm whether your devices are included in this recall.
2. **Replace Affected Pods**: If you have Pods from the identified lots, discontinue use right away and replace them with unaffected Pods. Insulet is offering free replacement Pods to impacted customers.
3. **Contact Support**: If you need help, reach out to Insulet Product Support at 1-800-641-2049. Live chat is also available at [omnipod.com/current-podders](https://omnipod.com/current-podders), and representatives are available 24/7.
## Stay Safe – Get Instant Recall Alerts
Medical device recalls such as this highlight the importance of staying informed. Staying proactive can help prevent health complications and ensure continued access to safe and functional medical devices.
**Call-to-Action (CTA)**: Download our app to receive real-time recall notifications for all your medical devices, prescriptions, and more. Don’t compromise on your health! Stay informed and protected.
For more information about Insulet Corporation and its innovative Omnipod® system, visit [insulet.com](https://insulet.com) or [omnipod.com](https://omnipod.com).
**Your safety is our priority.** Confirm your Omnipod® 5 Pods today and order your replacements if needed. Share this with other Omnipod® users to help spread the word!