Cardinal Healthcare recalls 15mg Meloxicam tablets due to potential temperature exposure during storage. Products may be affected if stored outside labeled conditions. Learn how to check and what to do.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling 15mg Meloxicam tablets that may have been exposed to temperatures outside their labeled storage conditions. This could affect product stability and safety, though the recall does not specify immediate harm.
The tablets may have been exposed to temperatures outside their labeled storage conditions during manufacturing. This could potentially affect product stability, though the recall does not indicate immediate harm or injury.
People who have prescription Meloxicam tablets from this manufacturer are affected. Those who store medications in uncontrolled environments may be at slightly higher risk.
Check for the product name 'Meloxicam Tablets, USP, 15 mg, 1000 Tablets per bottle' with NDC code 69097-159-15 and batch number KA11489. Products were manufactured by Cipla Ltd. in Kurkumbh, India and distributed by Cipla USA.
Look for the NDC code 69097-159-15 and batch number KA11489 on the product label.
The recall states potential temperature exposure but does not mention immediate harm or injury. The risk is considered low.
Check for the NDC code 69097-159-15 and batch number KA11489 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-0190-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0190-2024 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.
