Mckesson Medical-Surgical recalls Proventil HFA inhalers due to temperature abuse risks. Affected units may have been shipped with improper temperature control.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling Proventil HFA inhalers (Albuterol Sulfate) because of temperature abuse issues. This could lead to unsafe drug delivery if the inhaler is exposed to incorrect temperatures.
Temperature abuse means the inhaler may be exposed to temperatures that affect its stability. This could cause the medication to be less effective or unsafe for use.
Prescription inhaler users who received Proventil HFA from Mckesson Medical-Surgical. Those with the specific NDC 0085-1132-04 are most at risk.
Check for the NDC code 0085-1132-04 on the inhaler label. The product was distributed by Mckesson Medical-Surgical and may have been shipped with improper temperature control.
Look for the NDC code 0085-1132-04 on the inhaler label to confirm if it is affected.
The recall is due to temperature abuse issues that could affect the inhaler's stability and safety.
Check for the NDC code 0085-1132-04 on the inhaler label. The product was distributed by Mckesson Medical-Surgical.
The recall does not specify a remedy, so contact your pharmacy for guidance.
We’ve drafted a message you can send Mckesson Medical-Surgical to request your refund or repair — edit it as you like.
Subject: Recall D-1090-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1090-2022 from Mckesson Medical-Surgical. 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.
