Cardinal Healthcare recalls RIVASTIGMINE transdermal systems due to potential temperature exposure during storage. This may affect drug stability and safety for patients using the medication.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling RIVASTIGMINE transdermal systems that may have been exposed to temperatures outside the labeled storage conditions. This could affect the drug's stability and safety for patients using the medication.
The medication may have been exposed to temperatures outside the labeled storage conditions during production or distribution. This could potentially affect the drug's stability and safety, though the exact risk level is not specified in the recall notice.
Patients prescribed RIVASTIGMINE transdermal systems for nerve-related conditions. Those who have the specific product with NDC 47781-304-03 and batch P0248AL0AT are most at risk.
Check for the product name 'RIVASTIGMINE TRANSDERMAL SYSTEM' with 30 systems per box, NDC code 47781-3:04-03, and batch number P0248AL0AT. The product is distributed by Alvogen, Inc. in Morristown, NJ.
Verify the NDC code 47781-304-03 and batch number P0248AL0AT on the product label.
The recall states the product may have been exposed to temperatures outside labeled storage conditions, which could affect stability and safety. However, the exact risk level is not specified in the notice.
Look for the product name 'RIVASTIGMINE TRANSDERMAL SYSTEM' with 30 systems per box, NDC code 47781-304-03, and batch number P0248AL0AT.
The recall does not specify a remedy, so contact Cardinal Healthcare directly 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-0196-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0196-2024 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.
