Cardinal Healthcare recalls Inhub Wixela inhalers due to potential temperature exposure during storage. This may affect product stability. Consumers should check NDC 0378-9320-32 and batch 62002532.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling Inhub Wixel: a 500/50mcg fluticasone propionate and salmeterol inhalation powder with 60 doses. The recall is due to products being exposed to temperatures outside the labeled storage conditions, which could affect product stability.
The inhaler products were exposed to temperatures outside the labeled storage conditions during manufacturing. This could lead to reduced effectiveness of the medication or potential stability issues, though the risk of serious harm is low.
Current users of Inhub Wixela inhalers with NDC 0378-9320-32 and batch 62002532 are affected. Those with asthma or respiratory conditions are at slightly higher risk due to potential stability issues.
Check for the NDC code 0378-9320-32 and batch number 62002532 on the inhaler packaging. The product is labeled as Inhub Wixela (fluticasone propionate and salmeterol inhalation powder, USP) with 60 doses.
Look for NDC 0378-9320-32 and batch 62002532 on the inhaler packaging.
The recall is due to potential temperature exposure during manufacturing, which may affect product stability. However, the risk of serious harm is low.
Check for NDC 0378-9320-32 and batch 62002532 on the inhaler packaging.
The recall does not specify a remedy, so no action is required beyond checking the product details.
We’ve drafted a message you can send Cardinal Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0202-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0202-2024 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.
