Inventia Chlorthalidone Recall: Failed Dissolution Specs
Inventia Healthcare recalls 13,567 bottles of Chlorthalidone 25mg tablets due to failed dissolution specifications. Check your lot number and expiration date.
Use caution until it’s fixed
Failed Dissolution Specifications
What happened, in plain English
Inventia Healthcare Limited has recalled Chlorthalidone Tablets, USP, 25 mg because they failed dissolution specifications. This means the medication may not release its active ingredient properly, potentially affecting how well it works for patients. The recall covers 13,567 bottles distributed nationwide in the U.S. Read more at govinfonow.com/recall/1129584-inventia-chlorthalidone-recall-failed-dissolution-specs.
Source Summary by GovInfoNow · govinfonow.com/recall/1129584-inventia-chlorthalidone-recall-failed-dissolution-specs · Updated October 9, 2026 · FDA enforcement record: FDA #D-0852-2026
Cite this page
“Inventia Chlorthalidone Recall: Failed Dissolution Specs.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/1129584-inventia-chlorthalidone-recall-failed-dissolution-specs. Based on FDA recall #D-0852-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0852-2026%22&limit=1).
Why it’s dangerous
The tablets failed dissolution specifications, which is a quality control measure ensuring the drug breaks down correctly in the body. If the tablets do not dissolve properly, the patient may not receive the full dose of the medication, leading to ineffective treatment for their condition.
Who’s affected
Patients who have been prescribed Chlorthalidone Tablets, USP, 25 mg by Inventia Healthcare Limited and purchased them anywhere in the United States. Individuals with this specific lot number are at risk of receiving medication that may not work as intended.
How to tell if you have this one
Look for bottles containing Chlorthalidone Tablets, USP, 25 mg, manufactured by Inventia Healthcare Limited. Specifically check for NDC 64980-599-01, Batch # RISA24002, and an expiration date of 04/2027. The product was sold in bottles of 100 tablets.
- Brand
Inventia Healthcare- Category
Drug
What to do — step by step
Check Your Medication
Verify if your bottle matches NDC 64980-599-01, Batch # RISA24002, and Exp Date 04/2027.
Contact Your Pharmacist
Speak with your pharmacist or healthcare provider to determine the next steps for replacing this medication.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “U.S. 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 20 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
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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-0852-2026 (September 3, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0852-2026 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 9, 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.