Mckesson Medical-Surgical recalls certain Ipratropium Bromide 0.5mg and Albuterol Sulfate 3mg inhalation solutions due to temperature abuse risks. This affects prescription-only products with specific NDC numbers.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling specific prescription inhalation solutions that may have been exposed to improper temperatures. This could affect the medication's effectiveness and safety.
The medication may have been exposed to temperatures outside the recommended range during distribution. This could affect the stability and effectiveness of the inhalation solution, potentially leading to improper medication delivery.
Prescription patients who received these specific inhalation solutions from pharmacies. Those with the NDC numbers 0487-0201-03 (30-count) or 0487-0201-60 (60-count) are most at risk.
Check your prescription label for the NDC numbers 0487-0201-03 (30-count) or 0487-0201-60 (60-count). These products were distributed by Mckesson Medical-Surgical and are prescription-only.
Look for the NDC numbers 0487-0201-03 (30-count) or 0487-0201-60 (60-count) on the prescription label.
The recall is due to cGMP deviations related to temperature abuse during distribution, which could affect the medication's stability and effectiveness.
Check your prescription label for the NDC numbers 0487-0201-03 or 0487-0201-60. If you have these products, contact your pharmacy for guidance.
The recall covers products distributed by Mckesson Medical-Surgical with the specified NDC numbers, but no specific deadline is provided in the notice.
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-1021-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1021-2022 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.
