Dabur India recalls 144-count Med Pride Bacitracin Zinc Ointment due to FDA inspection findings of manufacturing deviations. Affected lots include 007, 008, 009, 015, 016. No specific remedy is stated in the recall notice.
CGMP Deviations; deficiencies observed during FDA inspection
Dabur India is recalling 144-count boxes of Med Pride Bacitracin Zinc Ointment because FDA inspections found manufacturing deviations. This recall does not include a specific action for consumers since the remedy is not stated.
The FDA identified manufacturing deviations during an inspection. These deviations could affect product quality and safety, but the specific risks are not detailed in the recall notice.
Owners of the recalled ointment boxes with lot numbers 007, 008, 009, 015, or 016 are affected. People using this product for skin care are most at risk if they have the affected lots.
Check for the lot numbers 007, 008, 009, 015, or 016 on the box. The product is a 144-count box of 0.9g packets with a net weight of 130g, manufactured in India.
Look for lot numbers 007, 008, 009, 015, or 016 on the box to determine if it is affected.
The recall notice does not state any specific remedy or action for consumers.
Lot numbers 007, 008, 009, 015, and 016 are affected.
Check for the lot numbers 007, 008, 009, 015, or 016 on the 144-count box of Med Pride Bacitracin Zinc Ointment.
We’ve drafted a message you can send Dabur India to request your refund or repair — edit it as you like.
Subject: Recall D-0635-2026 — Dabur India Dabur India Hello, I own a Dabur India that is covered by recall D-0635-2026 from Dabur India. 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.
