Cardinal Healthcare recalls lithium carbonate extended-release tablets due to potential temperature exposure during storage. This may affect safety if stored outside labeled conditions. Learn if you have affected products.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling lithium carbonate extended-release tablets that may have been exposed to temperatures outside the labeled storage conditions. This could pose a safety risk if the product is stored improperly.
The tablets may have been exposed to temperatures outside the labeled storage conditions during manufacturing. This could affect the product's stability and safety, though the risk is not severe under normal use conditions.
People with prescriptions for lithium carbonate extended-release tablets from Cardinal Healthcare. Those storing the product in environments with inconsistent temperatures are at slightly higher risk.
Check for the product name 'Lithium Carbonate Extended-Release Tablets, USP, 300 mg, 100 Tablets per bottle' with NDC code 0378-1300-01 and batch number 3138326. These were manufactured for Mylan Pharmaceuticals in Morgantown, WV.
Verify the NDC code 0378-1300-01 and batch number 3138326 on the product label.
The recall is due to potential temperature exposure during storage, but the product is generally safe if stored within labeled conditions. Consult your healthcare provider for specific advice.
Look for the NDC code 0378-1300-01 and batch number 3138326 on the product label. These tablets were manufactured for Mylan Pharmaceuticals in Morgantown, WV.
The recall does not specify a remedy, so check with your healthcare provider or the manufacturer 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-0189-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0189-2024 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.
