“Dr. Reddy's Tacrolimus Capsules 1mg Recall: Foreign Tablets Found.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/32924-dr-reddy-s-tacrolimus-capsules-1mg-recall-foreign-tablets-found. Based on FDA recall #D-0219-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0219-2024%22&limit=1).
Dr. Reddy's Laboratories, Inc. recalled Tacrolimus Capsels USP 1mg on Dec. 15, 2023, after the FDA announced the presence of foreign tablets in some bottles, according to FDA records.
The recall addresses the presence of foreign tablets or capsules, specifically one 0.5 mg Tacrolimus capsule found in a bottle of 1 mg Tacrolimus capsules.
Context
GovInfoNow's records show Dr. Reddy's Laboratories, Inc. has 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 Granules Pharmaceuticals Trazodone 50mg Recall (Jan. 26, 2026), Golden State Baclofen Tablets Recall (Nov. 26, 2025), and Annora Pharma Pitavastatin Tablets 2mg Recall (Feb. 3, 2026).
How to tell if you have this one
Check for the NDC number 55111-526-01 and lot number C2307275 on the bottle. The capsules are for prescription use only and expire in January 2026.
Brand
Dr. Reddy's
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check Capsule Contents
Inspect the bottle for foreign tablets inside the 1mg capsules. If found, do not use the bottle.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 9 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-0219-2024 (December 15, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0219-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.