Mckesson recalls Albuterol Sulfate Inhalation Solution 0.083% due to temperature abuse risks. This prescription-only product may be unsafe if stored improperly.
cGMP deviations: Temperature abuse
Mckesson is recalling Albuterol Sulfate Inhalation Solution 0.083% (2.5 mg/3mL) because of temperature abuse issues. This could lead to unsafe drug conditions if the product is stored incorrectly.
The product was manufactured with cGMP deviations related to temperature abuse. This means the inhaler could be unsafe if stored at incorrect temperatures, potentially causing the medication to degrade or become ineffective.
Prescription patients who received this specific Albuterol inhaler product from Mckesson. Those with medical conditions requiring inhalers are most at risk.
Check for Albuterol Sulfate Inhalation Solution 0.083% (2.5 mg/3mL) in 25 X 3mL unit-dose vials. This prescription-only product was distributed by Mckesson Medical-Surgical.
Identify if your inhaler matches the product description: Albuterol Sulfate Inhalation Solution 0.083%, 2.5 mg/3mL, 25 X 3mL unit-dose vials.
The recall states there were cGMP deviations related to temperature abuse, but the official notice does not specify if the product is safe to use.
Check for Albuterol Sulfate Inhalation Solution 0.083% (2.5 mg/3mL) in 25 X 3mL unit-dose vials, which were distributed by Mckesson Medical-Surgical.
The recall does not specify a remedy, so the official notice does not state what action to take.
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-1020-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1020-2022 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.
