Cardinal Healthcare recalls 875mg amoxicillin tablets due to potential temperature exposure during storage. This may affect product stability and safety.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling 875mg amoxicillin tablets that may have been exposed to temperatures outside their labeled storage conditions. This could affect product stability and safety.
The tablets were exposed to temperatures outside their labeled storage conditions during manufacturing. This could potentially affect the product's stability and safety, though the risk is not severe.
Prescription holders of the recalled amoxicillin tablets. Patients with specific medical conditions requiring precise medication timing may be at slightly higher risk.
Check for the product name 'Amoxicillin Tablets, USP, 875MG, 20 Tablets, Rx Only' with NDC code 0781-5060-20 and batch number LJ9004.
Verify the product name, NDC code, and batch number on the packaging to confirm if it matches the recalled items.
The product was exposed to temperatures outside of the labeled storage conditions during manufacturing, which could affect stability and safety.
Check for the product name 'Amoxicillin Tablets, USP, 875MG, 20 Tablets, Rx Only' with NDC code 0781-5060-20 and batch number LJ9004.
The recall does not specify a remedy, so check with your healthcare provider or pharmacist 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-0166-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0166-2024 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.
