Mckesson Medical-Surgical recalls Mupirocin Ointment 2% tubes due to temperature abuse risks. Patients should contact their pharmacy for safe handling instructions.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling Mupirocin Ointment 2% tubes (22g) that may have been exposed to improper temperatures. This could lead to ineffective treatment or safety risks if the ointment is not stored correctly.
The ointment may have been exposed to temperatures outside the recommended range during distribution. This could cause the medication to become ineffective or potentially unsafe if not stored properly.
Prescription patients using Mupirocin Ointment 2% tubes with NDC 0093-1010-42. Patients who have the product and are unsure about storage conditions are most at risk.
Check for the product name 'Mupirocin Ointment, USP 2%', 22 grams tube, NDC 0093-1010-42, and prescription label. The recall covers products distributed by McKesson Medical-Surgical.
Ensure the ointment is stored at the recommended temperature range to maintain effectiveness.
The recall indicates potential temperature abuse risks, but the product may still be safe if stored correctly. Consult your pharmacy for specific guidance.
Look for the product name 'Mupirocin Ointment, USP 2%', 22 grams tube, NDC 0093-1010-42, and prescription label.
Contact your pharmacy for instructions on safe handling or storage. The recall does not require immediate disposal.
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-1075-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1075-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
