Inventia Healthcare recalls Chlorthalidone Tablets, USP, 25 mg over failed dissolution specifications
The notice says these chlorthalidone tablets failed dissolution specifications, and it covers 13567 bottles of 100 tablets sold across the U.S.
What to do
The notice does not give instructions. Read the official notice for details.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Recall details
- Product
- Chlorthalidone Tablets, USP, 25 mg, 100 Tablets per bottle, Rx only, Manufactured by: Inventia Healthcare Limited. NDC: 64980-599-01
- Company
- Inventia Healthcare Limited
- Hazard
- Failed Dissolution Specifications
- Units
- 13567 bottles
- Where sold
- U.S. Nationwide
- FDA classification
- Class II · Ongoing
- Classified by FDA
- September 17, 2026
- Recall started
- September 3, 2026
- FDA enforcement report
- September 23, 2026
- Identifiers
- Codes: Batch # RISA24002; Exp Date: 04/2027
- FDA recall number: D-0852-2026
The headline, summary and steps above are written in plain English from the official notice below. Identifiers are copied exactly as the agency published them. Always check the official notice before you act.
Official notice
The notice's own wording from FDA.
- Product
- Chlorthalidone Tablets, USP, 25 mg, 100 Tablets per bottle, Rx only, Manufactured by: Inventia Healthcare Limited. NDC: 64980-599-01
- Reason for recall
- Failed Dissolution Specifications
- Classification
- Class II (Ongoing)
- Distribution
- U.S. Nationwide
- Quantity
- 13567 bottles
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