Cardinal Healthcare recalls 2mg Bumetanide tablets due to potential temperature exposure during storage. This may affect product stability and safety for patients using prescription medication.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling prescription 2mg Bumetanide tablets that may have been exposed to temperatures outside their labeled storage conditions. This could potentially affect the medication's stability and safety for patients using the prescription drug.
The tablets were exposed to temperatures outside their labeled storage conditions during manufacturing. This could potentially affect the medication's stability and safety for patients using the prescription drug.
Prescription patients using Bumetanide tablets manufactured by Amneal Pharmaceuticals Pvt. Ltd. in Ahmedabad, India, with batch number AM211171 are most at risk.
Check for Bumetanide Tablets, USP, 2 mg, 100 tablets per bottle, prescription-only, manufactured by Amneal Pharmaceuticals Pvt. Ltd. in Ahmedabad, India, with batch number AM211171.
Verify the product label for the batch number AM211171 and the manufacturer location in Ahmedabad, India.
The tablets were exposed to temperatures outside their labeled storage conditions during manufacturing, which could affect stability and safety.
The recall record does not specify a remedy, so check the product details to confirm if it's affected and contact your healthcare provider for guidance.
The recall indicates potential temperature exposure, but the record does not specify serious injury risks or immediate action needed.
We’ve drafted a message you can send Cardinal Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0171-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0171-2024 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.
