Cardinal Healthcare recalls 20mg Citalopram tablets due to potential temperature exposure during storage. This may affect product stability. Consumers should check NDC 0378-6232-01 and batch 3131748.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling 20mg Citalopram tablets that may have been exposed to temperatures outside their labeled storage conditions. This could affect product stability and safety for patients using these prescription medications.
The tablets were exposed to temperatures outside their labeled storage conditions during manufacturing. This could potentially affect product stability, though the recall does not indicate immediate harm to users.
Prescription patients who have the specific 20mg Citalopram tablets with NDC 0378-6232-01 and batch 3131748. Those with the medication at home are most at risk.
Check for the NDC code 0378-6232-01 and batch number 3131748 on the packaging. These tablets are prescription-only and manufactured by Mylan Pharmaceuticals Inc. in Morgantown, WV.
Look for the NDC code 0378-6232-01 and batch number 3131748 on the tablet packaging.
The recall does not indicate immediate harm, but the product may have been exposed to temperatures outside labeled storage conditions, so it's recommended to check the packaging details.
Check for the NDC code 0378-6232-01 and batch number 3131748 on the packaging. These tablets are prescription-only and manufactured by Mylan Pharmaceuticals Inc. in Morgantown, WV.
The recall does not specify a remedy, so check the packaging details to confirm and contact your healthcare provider 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-0173-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0173-2024 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.
