Cardinal Healthcare recalls Warfarin Sodium Tablets due to potential temperature exposure during storage. This may affect product stability. Check NDC 0093-1714-01 and batch 2169041 for affected items.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling Warfarin Sodium Tablets that may have been exposed to temperatures outside their labeled storage conditions. This could affect product stability, but the recall does not indicate immediate safety risks to users.
The tablets may have been exposed to temperatures outside their labeled storage conditions during manufacturing or distribution. This could potentially affect the product's stability, but the recall does not specify a direct safety risk to users.
People with prescriptions for Warfarin Sodium Tablets, especially those using the product as directed by their healthcare provider. Patients on blood thinner therapy are most at risk if the product is unstable.
Check for Warfarin Sodium Tablets, USP, 2.5 mg, 100 tablets per bottle, with NDC code 0093-1714-01 and batch number 2169041. These were manufactured for Teva Pharmaceuticals in Parsippany, NJ.
Look for the NDC code 0093-1714-01 and batch number 2169041 on the product label.
The recall does not indicate immediate safety risks, but the product may have been exposed to temperatures outside labeled storage conditions, potentially affecting stability.
Check for Warfarin Sodium Tablets, USP, 2.5 mg, 100 tablets per bottle with NDC 0093-1714-01 and batch 2169041.
The recall does not specify a remedy, so contact your healthcare provider for guidance on whether to continue using the product.
We’ve drafted a message you can send Cardinal Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0200-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0200-2024 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.
