Cardinal Healthcare recalls 100-tablet bottles of Lisinopril and Hydrochlorothiazide tablets due to potential temperature exposure during storage, which may affect product stability.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling Lisinopril and Hydrochlorothiazide tablets that were exposed to temperatures outside their labeled storage conditions. This could affect the medication's stability and safety, so affected users should contact the manufacturer for instructions.
The medication was exposed to temperatures outside the labeled storage conditions during manufacturing. This could potentially affect the stability of the tablets, though the exact impact on safety is not specified in the recall.
People who have prescription bottles of Lisinopril and Hydrochlorothiazide tablets (10mg/12.5mg, 100 tablets per bottle) manufactured by Lupin for Cardinal Healthcare. Those with specific batch numbers Q101699 or Q101981 are most at risk.
Check for bottles labeled 'Lisinopril and Hydrochlorothiazide Tablets USP, 10mg/12.5mg, Rx only, 100 Tablets per bottle' from Cardinal Healthcare, manufactured by Lupin. Look for batch numbers Q101699 or Q101981 on the packaging.
Identify the batch number on the packaging to confirm if it matches Q101699 or Q101981.
The medication was exposed to temperatures outside the labeled storage conditions during manufacturing, which could affect its stability.
Contact Cardinal Healthcare directly to confirm if your specific batch is affected and follow their instructions.
The recall indicates potential stability issues, but no specific safety risks are mentioned in the official notice.
We’ve drafted a message you can send Cardinal Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0188-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0188-2024 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.
