Cardinal Healthcare recalls folic acid tablets due to potential temperature exposure during storage. Products may not meet quality standards if stored outside labeled conditions.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling folic acid tablets that could be affected by improper storage temperatures. This recall is for products that may not meet quality standards if stored outside the labeled conditions.
The tablets were exposed to temperatures outside the labeled storage conditions during manufacturing, which could affect their quality. This may lead to the tablets not meeting the required standards for safe use.
People who have the specific folic acid tablets with NDC 69315-127-10 and batch H08221, typically prescribed by a healthcare provider. Those storing the tablets in non-ideal temperatures are at higher risk.
Check for the product name 'Folic Acid Tablets, USP, 1MG, 100 Tablets per bottle' with NDC code 69315-127-10 and batch number H08221. These were manufactured by Leading Pharma, LLC in Fairfield, NJ.
Verify the NDC code 69315-127-10 and batch number H08221 on the product label.
The product was exposed to temperatures outside the labeled storage conditions during manufacturing, which may affect quality.
Look for the NDC code 69315-127-10 and batch number H08221 on the product label.
The recall does not specify a remedy, so contact your healthcare provider 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-0183-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0183-2024 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.
