Mckesson Medical-Surgical recalls Triple Antibiotic Ointment due to improper storage conditions. Products may not meet drug label specifications, potentially affecting safety.
CGMP Deviations: products were stored outside the drug label specifications.
Mck: Mckesson Medical-Surgical recalls Triple Antibiotic Ointment because it was stored outside drug label specifications. This could mean the product doesn't meet safety standards, but the recall doesn't specify immediate harm.
The ointment was stored outside the required drug label specifications, which could lead to the product not meeting safety standards. This might affect the product's effectiveness or safety, but the recall doesn't specify immediate harm.
People who own or use Triple Antibiotic Ointment from this manufacturer are affected. Those using the product for medical purposes may be at slightly higher risk due to storage issues.
Check for the product name 'Triple Antibiotic Ointment' or similar names. Look for the NDC code 0498-0750-36 on the packaging. Products were sold by Honeywell Safety Products.
Look for the NDC code 0498-0750-36 on the packaging to confirm if it's recalled.
The recall states the product was stored outside drug label specifications, but it doesn't specify immediate danger or injury. The product may not meet safety standards.
Check for the NDC code 0498-0750-36 on the packaging. Products were sold by Honeywell Safety Products.
The recall doesn't provide specific action steps. Check the product details to confirm and contact the manufacturer for further guidance.
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-1311-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1311-2022 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.
