Dabur India Limited recalls Med Pride triple antibiotic ointment due to FDA inspection findings of manufacturing deviations. Affected lots from 011 to 022 and 026, sold in 144-packet boxes.
CGMP Deviations; deficiencies observed during FDA inspection
Dabur India Limited is recalling Med Pride triple antibiotic ointment because FDA inspections found manufacturing deviations. This could affect product safety and quality.
The FDA identified manufacturing deviations during an inspection. These deviations could impact product safety and quality, but the specific risks are not detailed in the recall notice.
Owners of the recalled ointment, particularly those who purchased it from U.S. retailers. People using the product for medical purposes may be at risk.
Check for the product name 'Med Pride' on the label. Look for lot numbers 011 through 022 and 026 on the packaging. The product comes in 144-packet boxes with a weight of 130g.
Identify the lot number on the packaging to confirm if it's affected (011 to 022 and 026).
The recall notice states there were manufacturing deviations found by FDA, but does not specify if the product is safe to use.
The recall notice does not provide specific action steps for affected products.
Check the lot number on the packaging; affected lots are 011 through 022 and 026.
We’ve drafted a message you can send Dabur to request your refund or repair — edit it as you like.
Subject: Recall D-0641-2026 — Dabur Dabur Hello, I own a Dabur that is covered by recall D-0641-2026 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.
