Lower riskDrug recall · FDA · Published April 15, 2022
Dr. Reddy's Lansoprazole Tablets Recall: Failed Dissolution Risk
Dr. Reddy's recalls 30mg Lansoprazole tablets due to failed dissolution specifications. This may affect medication effectiveness. Check your product details and contact the manufacturer for guidance.
“Dr. Reddy's Lansoprazole Tablets Recall: Failed Dissolution Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/34833-dr-reddy-s-lansoprazole-tablets-recall-failed-dissolution-risk. Based on FDA recall #D-0853-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0853-2022%22&limit=1).
The FDA announced on April 15, 2022, that Dr. Reddy's Laboratories, Inc. voluntarily recalled Lansoprazole Delayed-Release Orally Disintegrating Tablets due to failed dissolution specifications. The recall affects 252 blister packs distributed in Ohio.
Packaging: 10 Packs of 10 Tablets each, 100 Tablets per blister pack
NDC: 43598-561-78
Lot #: T2000645
Expiration Date: 07/2022
Quantity: 252 Blister Packs
Distribution: Ohio
The hazard
The recalled Lansoprazole tablets failed to meet dissolution specifications. The FDA classified this recall as Class II.
Context
GovInfoNow's records show Dr. Reddy's Laboratories, Inc. has had 85 other recalls on record since April 9, 2012. Other recent recalls of similar products include Dr. Reddy's Varenicline Tablets Recall (Nov. 11, 2025), Dr. Reddy's Succinylcholine Chloride Injection Recall (Sept. 26, 2025), and Dr. Reddy's Omeprazole Capsules Recall (June 30, 2025). Other recent recalls of similar products include AvKARE Rosuvastatin Tablets 10mg Recall (Dec. 31, 2025), Lannett Niacin Extended-release Tablets Recall (May 27, 2026), and Teva Metoprolol Succinate Tablets Recall (Jan. 29, 2026).
How to tell if you have this one
Look for the product name 'Lansoprazole Delayed-Release Orally Disintegrating Tablets, 30 mg' with 10 packs of 10 tablets per blister. The lot number T2000645 and expiration date 07/2022 are also key identifiers.
Brand
Dr. Reddy's
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check Product Details
Verify the product name, lot number T2000645, and expiration date 07/2022 to confirm if it's recalled.
Where it went and when
Where it was distributed
Distributed in Ohio.
Listed by the agency
Not listed
FDA distribution: “OH” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Ohio.
Recall timeline
FDA terminated this recall 19 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #D-0853-2022 (April 15, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0853-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.