Dr. Reddy's recalls 15mg Lansoprazole Delayed-Release Capsules due to failed dissolution specifications in long-term stability testing. This affects specific bottle counts and expiration dates.
Failed Dissolution Specifications; during long term stability testing.
Dr. Reddy's is recalling 15mg Lansoprazole Delayed-Release Capsules that failed dissolution testing during long-term stability checks. This means the medication may not work as intended, but the recall does not indicate immediate safety risks.
The capsules failed dissolution testing during long-term stability testing, meaning they may not release the medication properly in the stomach. This could lead to the medication not working as intended, but it does not pose a direct safety risk like injury or death.
People who have the 30-count or 90-count bottles of 15mg Lansoprazole Delayed-Release Capsules with the specified NDC numbers and expiration dates are affected. Those using prescription medication for acid reflux or ulcers are most at risk.
Check for 15mg Lansoprazole Delayed-Release Capsules in 30-count (NDC 55111-398-30) or 90-count (NDC 55111-398-90) bottles. The expiration dates are December 2023 for both lots.
Verify the bottle count and NDC number to confirm if your product is affected.
The recall is due to failed dissolution testing, which may affect medication effectiveness, but it does not indicate immediate safety risks.
The recall does not specify a remedy, so check with your doctor or pharmacist for guidance on whether to continue using the product.
The recall indicates potential medication effectiveness issues, but no immediate safety risks like injury or death are mentioned.
We’ve drafted a message you can send Dr. Reddy's to request your refund or repair — edit it as you like.
Subject: Recall D-0737-2022 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0737-2022 from Dr. Reddy's. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
