Cardinal Healthcare recalls 37.5 mg/25 mg Triamterene and Hydrochlorothiazide capsules due to potential temperature exposure during storage, risking product instability. Rx-only medication distributed by Lannett Company.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling triamterene and hydrochlorothiazide capsules that may have been exposed to temperatures outside their labeled storage conditions. This could affect product stability, though the recall does not indicate immediate safety risks to users.
The capsules were exposed to temperatures outside their labeled storage conditions during manufacturing or distribution. This could potentially affect product stability, but the recall does not indicate immediate safety risks to users.
Prescription users of triamterene and hydrochlorothiazide capsules who received this specific product from Lannett Company. Patients on blood pressure or fluid management medications are most at risk if they have the recalled batch.
Check for the product name 'Triamterene and Hydrochlorothiazide Capsules, USP, 37.5 mg/25 mg, 100 capsules per bottle' with NDC code 0527-1632-01 and batch numbers 21000279A or 21000280A. These were distributed by Lannett Company, Inc in Philadelphia, PA.
Verify the NDC code 0527-1632-01 and batch numbers 21000279A or 21000280A on the bottle.
The recall does not indicate immediate safety risks, but the product may have been affected by temperature exposure during storage.
Check for the NDC code 0527-1632-01 and batch numbers 21000279A or 21000280A on the bottle, which were distributed by Lannett Company, Inc.
The recall does not specify a remedy, so contact Cardinal Healthcare directly for guidance.
We’ve drafted a message you can send Cardinal Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0199-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0199-2024 from Cardinal 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.
