Cardinal Healthcare recalls fluticasone nasal spray due to potential temperature exposure during storage. Products may be affected if stored outside labeled conditions. Check NDC 60505-0829-1 batch TE9159 or TE8156.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling fluticasone nasal spray products that may have been exposed to temperatures outside the labeled storage conditions. This could affect product stability and safety, though the recall does not specify a risk of serious injury.
The spray may have been exposed to temperatures outside the labeled storage conditions during manufacturing, which could affect product stability. This might lead to reduced effectiveness or potential safety issues, but the recall does not indicate a risk of serious injury.
People with prescriptions for this nasal spray, particularly those who store it in uncontrolled environments. Those who have the specific NDC 60505-0829-1 batch TE9159 or TE8156 products are most at risk.
Check for the NDC code 60505-0829-1 and batch numbers TE9159 or TE8156 on the product label. The product is a fluticasone nasal spray with 50mcg per spray, 120 doses, and is prescription-only.
Look for the NDC code 60505-0829-1 and batch numbers TE9159 or TE8156 on the product label.
The recall does not indicate a risk of serious injury, but the product may have been affected by temperature exposure during storage.
Check for the NDC code 60505-0829-1 and batch numbers TE9159 or TE8156 on the product label.
The recall does not specify a remedy, so contact Cardinal Healthcare for further instructions.
We’ve drafted a message you can send Cardinal Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0182-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0182-2024 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.
