Dr. Reddy's recalls 35mg Lansop: tablets may not dissolve properly, causing ineffective treatment. Check NDC 43598-561-78 or lot T2100515 for affected products.
FAILED DISSOLUTION SPECIFICATIONS
Dr. Reddy's is recalling 35mg Lansoprazole Delayed-Release Orally Disintegrating Tablets that may not dissolve properly. This could lead to ineffective treatment of acid reflux. Affected products have specific lot numbers and NDC codes.
The tablets may not dissolve properly in the mouth, leading to ineffective treatment of acid reflux. This could cause the medication not to work as intended.
People who have the 35mg Lansoprazole tablets with NDC 43598-561-78 and lot T2100515 are affected. Those taking this medication for acid reflux are most at risk.
Check the blister pack for NDC 43598-561-78 and lot number T2100515. Products sold in the U.S. with this specific lot number are affected.
Look for NDC 43598-561-78 and lot number T2100515 on the blister pack.
The tablets failed dissolution specifications, meaning they may not dissolve properly in the mouth, leading to ineffective treatment.
Check the product details for NDC 43598-561-78 and lot number T2100515. If you have the affected product, contact Dr. Reddy's for guidance.
The recall is for ineffective treatment, not a risk of serious injury. The danger level is low risk.
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-1288-2022 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-1288-2022 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.
