Cardinal Healthcare recalls ALBUTEROL SULFATE HFA inhalers due to temperature exposure during manufacturing. Products may be affected by improper storage conditions.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling ALBUTEROL SULFATE HFA inhalers that were exposed to temperatures outside their labeled storage conditions. This could affect product stability and safety for users.
The inhalers were manufactured under conditions where they were exposed to temperatures outside the labeled storage range. This could potentially affect the product's stability and effectiveness, though serious injury is not expected.
People with prescriptions for this inhaler, particularly those using it for asthma or COPD. Those who have the specific product model and batch number are most at risk.
Check for the product name 'ALBUTEROL SULFATE HFA Inhalation Aerosol', 90mcg per actuation, 200 metered inhalations, net weight 18g, and the batch number MY7E. These products were manufactured by Prasco Laboratories in Mason, OH.
Verify the product name, model, and batch number (MY7E) to confirm if it's affected.
The recall indicates potential temperature exposure during manufacturing, but the product is still safe to use if stored properly. Consult your healthcare provider for guidance.
Check the product details to confirm if it's affected. If it is, contact Cardinal Healthcare for further instructions.
Look for the product name 'ALBUTEROL SULFATE HFA Inhalation Aerosol', 90mcg per actuation, 200 metered inhalations, net weight 18g, and batch number MY7E.
We’ve drafted a message you can send Cardinal Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0162-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0162-2024 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.
