Mckesson Medical-Surgical recalls Azithromycin for Injection USP vials due to temperature abuse risks. Affected products may have been shipped without proper temperature control.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling Azithromycin for Injection USP vials (500 mg) because they may have been exposed to improper temperatures during shipping. This could lead to ineffective medication or safety risks if the vials are used without proper temperature control.
The vials may have been exposed to temperatures outside the required range during shipping, which can compromise the medication's stability. This could result in the drug being ineffective or potentially unsafe if used without proper temperature control.
Healthcare providers and patients who received the recalled Azithromycin for Injection USP vials from Mckesson Medical-Surgical. Those using the product without verifying the lot number are at risk of receiving ineffective medication.
Check for the product name 'Azithromycin for Injection USP Vial, 500 mg per vial' and the NDC code 55150-174-10. The recall affects products distributed by Mckesson Medical-Surgical without a specific lot number identified for each customer.
Verify the NDC code 55150-174-10 and product name to confirm if you have the recalled Azithromycin for Injection USP vial.
The recall is due to potential temperature abuse during shipping, which may compromise the medication's stability.
Check for the NDC code 55150-174-10 and product name 'Azithromycin for Injection USP Vial, 500 mg per vial' from Mckesson Medical-Surgical.
The recall does not specify a remedy, so contact Mckesson Medical-Surgical to verify if you have the affected product.
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-0997-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-0997-2022 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.
