Cardinal Healthcare recalls 5mg Aripiprazole tablets (NDC 65162-897-03) produced in 2023 that may have been exposed to improper temperatures. Consumers should check product details and contact Cardinal Healthcare for guidance.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling 5mg Aripiprazole tablets that may have been exposed to temperatures outside the labeled storage conditions. This could potentially affect product stability and safety, though the recall does not specify immediate harm.
The tablets were exposed to temperatures outside the labeled storage conditions during manufacturing. This could potentially affect the product's stability and safety, though the recall does not specify immediate harm or injury.
People who own or use the recalled 5mg Aripiprazole tablets (NDC 65162-897-03) produced in 2023. Those most at risk are individuals taking the medication who may have stored it improperly.
Check for the NDC code 65162-897-03 and batch number AR202318 on the product label. The tablets were distributed by Amneal Pharmaceuticals LLC in Bridgewater, NJ.
Look for the NDC code 65162-897-03 and batch number AR202318 on the product label.
The recall states the tablets may have been exposed to improper temperatures, but does not specify immediate harm or injury.
Check for the NDC code 65162-897-03 and batch number AR202318 on the product label.
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-0167-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0167-2024 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.
