Mckesson Medical-Surgical recalls Metronidazole Vaginal Gel USP 0.75% with 5 applicators due to temperature abuse during storage. This prescription product may be unsafe if exposed to improper temperatures.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling Metronidazole Vaginal Gel USP 0.75% with 5 applicators because of temperature abuse issues. This could lead to unsafe product conditions if the gel is stored at incorrect temperatures.
The product was manufactured with cGMP deviations related to temperature abuse. This means the gel may not be safe if stored or handled at temperatures that could compromise its stability.
Prescription patients who received this specific Metronidazole Vaginal Gel product from a pharmacy. Those using the product without proper temperature control are at higher risk.
Check for the product name 'Metronidazole Vaginal Gel USP 0.75% with 5 applicators', net weight 70g tube, and NDC 0781-7077-87. The product is prescription-only and was distributed by McKesson Medical-Surgical.
Look for the product name, net weight 70g tube, and NDC 0781-7077-87 on the label.
The recall indicates potential temperature abuse issues, but the product may still be safe if stored properly. Consult your healthcare provider for specific guidance.
Check for the product name 'Metronidazole Vaginal Gel USP 0.75% with 5 applicators', net weight 70g tube, and NDC 0781-7077-87.
The recall does not specify a remedy, so contact your pharmacy or healthcare provider for advice.
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-1048-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1048-2022 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.
