Dabur India Limited recalls 500 Med Pride Bacitracin Zinc Ointment tubes (1oz) due to FDA inspection findings of manufacturing deviations. Affected lots include 001-020. Consumers should check product details and contact Dabur for guidance.
CGMP Deviations; deficiencies observed during FDA inspection
Dabur India Limited is recalling 500 tubes of Med Pride Bacitracin Zinc Ointment because FDA inspections found manufacturing deviations. This recall affects specific production lots made in India with certain UPC codes. The issue could lead to product quality problems but does not involve immediate safety risks.
The FDA identified manufacturing deviations during an inspection. These deviations could result in the ointment not meeting quality standards, potentially affecting its effectiveness or safety. However, the recall does not indicate a risk of serious injury or harm.
Owners of the recalled Med Pride Bacitracin Zinc Ointment tubes (1oz) with lot numbers 001-020 are affected. People using these products for skin care are most at risk of receiving substandard medication.
Check for the product name 'Med Pride Bacitracin Zinc Ointment', 1oz (28.3g) tubes, and lot numbers 001 through 020. The product was manufactured in India and sold with UPC code 3 52410 30354 8.
Look for the lot numbers 001-020 on the tube to confirm if your product is affected.
The FDA found manufacturing deviations during an inspection, which could affect the product's quality but does not indicate an immediate safety risk.
Check for lot numbers 001-020 on the tube. The product was manufactured in India and sold with UPC code 3 52410 30354 8.
The recall does not specify a remedy, so contact Dabur India Limited directly for guidance.
We’ve drafted a message you can send Dabur to request your refund or repair — edit it as you like.
Subject: Recall D-0636-2026 — Dabur Dabur Hello, I own a Dabur that is covered by recall D-0636-2026 from Dabur. 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.
