Mckesson recalls albuterol inhalers due to temperature abuse risks. Products may have been shipped with improper temperature control, potentially affecting safety.
cGMP deviations: Temperature abuse
Mckesson is recalling albuterol inhalers that may have been exposed to improper temperatures during shipping. This could lead to unsafe product conditions, but the recall does not specify a direct risk of injury.
The inhaler may have been exposed to temperatures that cause the product to become unstable. This could lead to inconsistent dosing or other safety issues, though the exact mechanism is not detailed in the recall.
Prescription holders of albuterol inhalers with the specific NDC code 0254-1007-52. Patients using these inhalers for asthma or respiratory conditions are most at risk if the product was improperly stored.
Check for the NDC code 0254-1007-52 on the inhaler label. Products were manufactured for PAR Pharmaceutical and distributed by Mckesson Medical-Surgical.
Look for the NDC code 0254-1007-52 on the inhaler label to confirm if it is recalled.
The recall indicates potential temperature abuse risks, but the official notice does not specify if the product is unsafe to use. Check the label for the NDC code to determine if it is recalled.
Look for the NDC code 0254-1007-52 on the inhaler label. Products were manufactured for PAR Pharmaceutical and distributed by Mckesson Medical-Surgical.
The recall does not specify a remedy, so contact Mckesson Medical-Surgical for further instructions if you have the NDC code 0254-1007-52.
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-1023-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1023-2022 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.
