Cardinal Healthcare recalls 300ml Lansoprazole 3mg/ml (Rx only) due to temperature exposure during storage. Products may be unsafe if stored outside labeled conditions.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling a specific 300ml Lansoprazole medication because it was exposed to temperatures outside the labeled storage conditions. This could potentially make the product unsafe if stored improperly.
The medication was exposed to temperatures outside the labeled storage conditions during manufacturing. This could lead to the product being unstable or ineffective if stored improperly.
People who have a prescription for this specific Lansoprazole product are affected. Those who store the medication in uncontrolled environments are at higher risk.
Check for the product name 'Lansoprazole 3mg/ml 300ml', prescription-only status, and the NDC code 65628-080-10. The batch number is 21025A.
Ensure the medication is stored at the temperature specified on the label to maintain safety.
The product may be unsafe if stored outside the labeled temperature conditions. Always check storage instructions.
Look for the product name 'Lansoprazole 3mg/ml 300ml', prescription-only status, NDC 65628-080-10, and batch number 21025A.
Check if the product was stored at the correct temperature. If unsure, contact your pharmacist or healthcare provider.
We’ve drafted a message you can send Cardinal Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0181-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0181-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.