Dr. Reddy's Tizanidine Tablets Recall: Foreign Tablets Risk
Dr. Reddy's recalls 4mg tizanidine tablets with foreign 2mg tablets. Consumers should check NDC 55111-180-15 and lot T2304007 for affected products.
Lower-risk recall
Presence of Foreign tablets/capsules - identified as tizanidine 2 mg tablets.
Contact the company
What happened, in plain English
Dr. Reddy's is recalling 4mg tizanidine tablets that contain foreign 2mg tablets. This could cause incorrect dosing if taken without knowing the tablet's actual strength. Read more at govinfonow.com/recall/32894-dr-reddy-s-tizanidine-tablets-recall-foreign-tablets-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/32894-dr-reddy-s-tizanidine-tablets-recall-foreign-tablets-risk · Updated August 17, 2026 · FDA enforcement record: FDA #D-0223-2024
Cite this page
“Dr. Reddy's Tizanidine Tablets Recall: Foreign Tablets Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/32894-dr-reddy-s-tizanidine-tablets-recall-foreign-tablets-risk. Based on FDA recall #D-0223-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0223-2024%22&limit=1).
Why it’s dangerous
The tablets contain foreign 2mg tizanidine tablets that could lead to incorrect dosing if taken without knowing the tablet's actual strength. This may cause underdosing or overdosing depending on the patient's condition.
Who’s affected
People who have the specific 150-count bottle with NDC 55111-180-15 and lot number T2304007. Prescriptions for tizanidine are typically for medical use only.
How to tell if you have this one
Check for the NDC code 55111-180-15 and lot number T2304007 on the bottle. The product is a 150-count bottle of tizanidine 4mg tablets, prescription-only.
- Brand
Dr. Reddy's- Category
Drug
What to do — step by step
Check Product Details
Look for NDC 55111-180-15 and lot number T2304007 on the bottle.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “USA Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 15 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Questions people ask
What should I do if I have this product?
Check the product details to see if it matches the recalled batch. If it does, contact Dr. Reddy's for further instructions.
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Where this comes from
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-0223-2024 (January 2, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0223-2024 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.