Mckesson Medical-Surgical recalls Ipratropium Bromide Inhalation Solution due to temperature abuse risks. This prescription-only medication may be affected by improper storage conditions.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling a specific prescription inhaler product because of temperature abuse risks. This means the medication could be affected if stored at incorrect temperatures, potentially reducing its effectiveness.
The medication may be affected by temperature abuse, meaning improper storage could reduce its effectiveness. This is a cGMP (current Good Manufacturing Practice) deviation that affects the product's quality and safety.
Prescription patients who have the specific 0.02% Ipratropium Bromide Inhalation Solution (25-count box) are affected. Patients using this medication for respiratory conditions are most at risk if the product was stored improperly.
Check for the 25-count box labeled 'Ipratropium Bromide Inhalation Solution, 0.02%, 0.5 mg/2.5 mL' with NDC 0487-9801-25. This prescription-only product was distributed by Mckesson Medical-Surgical.
Verify the product label includes 'Ipratropium Bromide Inhalation Solution, 0.02%, 0.5 mg/2.5 mL' in a 25-count box with NDC 0487-9801-25.
The product may be affected by temperature abuse, which could reduce effectiveness. Patients should check storage conditions and contact their healthcare provider.
Look for the 25-count box labeled 'Ipratropium Bromide Inhalation Solution, 0.02%, 0.5 mg/2.5 mL' with NDC 0487-9801-25.
The recall does not specify a remedy, so patients should check with their healthcare provider about proper storage and use.
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-1040-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1040-2022 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.
