Cardinal Healthcare recalls Warfarin Sodium 5mg tablets due to potential temperature exposure during storage. This may affect product stability and safety for patients on blood thinners.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling Warfarin Sodium Tablets (5 mg, 100 per bottle) because they may have been exposed to temperatures outside the labeled storage conditions. This could affect the medication's stability and safety for patients using blood thinners.
Warfarin tablets can lose potency or become unstable if exposed to temperatures outside the labeled storage range. This could lead to ineffective blood thinning or other safety issues for patients using the medication.
Patients prescribed warfarin for blood clotting who use the recalled tablets. Those with specific storage conditions not met may be at higher risk.
Check for the product name 'Warfarin Sodium Tablets, USP, 5 mg, 100 Tablets per bottle' with NDC code 0093-1721-01 and batch number 2323041. The product was manufactured for Teva Pharmaceuticals in Parsippany, NJ.
Verify the NDC code 0093-1721-01 and batch number 2323041 on the product label.
The recall indicates potential temperature exposure, which could affect stability. Patients should contact their healthcare provider for guidance.
Check for the NDC code 0093-1721-01 and batch number 2323041 on the product label.
The recall does not specify a remedy, so contact your healthcare provider for advice on next steps.
We’ve drafted a message you can send Cardinal Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0201-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0201-2024 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.
