Cardinal Healthcare recalls ALBUTEROL SULFATE inhalers exposed to improper temperatures. This may affect product stability and safety. Learn if your inhaler is affected and what to do.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling ALBUTEROL SULFATE inhalers that may have been exposed to temperatures outside their labeled storage conditions. This could potentially affect product stability and safety, though the recall does not specify a risk of serious injury.
The inhalers may have been exposed to temperatures outside their labeled storage conditions during manufacturing. This could potentially affect product stability and safety, though the recall does not specify a risk of serious injury.
People with prescriptions for ALBUTEROL SULFATE inhalers manufactured by Lupin for Cardinal Healthcare. Those with medical conditions requiring inhalers are most at risk.
Check for the product name 'ALBUTEROL SULFATE', 90mcg per actuation, 200 metered inhalations, Rx only, 8.5g net weight. The NDC code is 68180-963-01 and batch number K100715.
Identify the product name, strength, and batch number to confirm if it's affected.
The recall states the product may have been exposed to improper temperatures, but does not specify a risk of serious injury.
Check for the product name 'ALBUTEROL SULFATE', 90mcg per actuation, 200 metered inhalations, Rx only, 8.5g net weight, NDC 68180-963-01, and batch K100715.
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-0163-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0163-2024 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.
