Inventia Healthcare recalls 25mg Chlorthalidone tablets due to failed dissolution specifications. Rx-only medication with specific batch numbers and expiration dates. Consumers should contact the manufacturer for details.
Failed Dissolution Specifications
Inventia Healthcare is recalling 25mg Chlorthalidone tablets that failed dissolution specifications. This means the medication may not work as intended, which could affect blood pressure treatment. The recall applies to specific batch numbers and expiration dates.
The tablets failed dissolution specifications, meaning they may not release the medication properly in the body. This could lead to ineffective blood pressure control. However, the recall is for prescription-only medication with specific batch numbers.
People who have prescription Chlorthalidone tablets from Inventia Healthcare with the specified batch numbers and expiration dates. Those taking blood pressure medication are most at risk if the tablets don't dissolve properly.
Check for the product name 'Chlorthalidone Tablets, USP, 25 mg' on the label. Look for batch numbers RISA24001 (100 tablets) or RISB24002 (1000 tablets) and expiration date 04/2027.
Identify the batch number and expiration date on the label to confirm if the product is recalled.
The tablets failed dissolution specifications, meaning they may not release the medication properly in the body.
Contact Inventia Healthcare directly for instructions on what to do with the product.
Yes, avoid batch numbers RISA24001 (100 tablets) and RISB24002 (1000 tablets).
We’ve drafted a message you can send Inventia Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0610-2026 — Inventia Healthcare Inventia Healthcare Hello, I own a Inventia Healthcare that is covered by recall D-0610-2026 from Inventia Healthcare. 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.
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