Mckesson recalls albuterol inhalers due to temperature abuse risks. This affects prescription-only 0.021% solution in 30 vials. No specific remedy provided in the recall notice.
cGMP deviations: Temperature abuse
Mckesson is recalling prescription albuterol inhalers that may have been exposed to improper temperatures. This could cause the medication to become unstable, potentially affecting its safety and effectiveness.
The medication may have been exposed to temperatures that cause instability. This could lead to improper drug concentration or effectiveness, but the recall does not specify if this poses a serious injury risk.
Prescription holders of albuterol inhalers with the specific packaging described. Patients using these inhalers for asthma or respiratory conditions are at risk if the product was exposed to temperatures outside the recommended range.
Check for albuterol inhalers labeled 0.021%, 0.63 mg/3mL, in 30 x 3 mL vials. These are prescription-only products with NDC 0487-0301-01. The recall does not specify a particular lot number or distribution date.
Look for the product label with the specific concentration and packaging described in the recall.
The recall notice does not provide a specific remedy or action for consumers.
Check for albuterol inhalers labeled 0.021%, 0.63 mg/3mL, in 30 x 3 mL vials. The recall does not specify a particular lot number or distribution date.
The recall indicates potential temperature abuse issues, but does not specify if this poses a serious injury risk.
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-1018-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1018-2022 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.
