Dabur India Limited recalls Med Pride hydrocortisone cream 1% tubes (1 oz) due to FDA inspection findings of manufacturing deviations. Affected lots include 001, 002, 013, 016, 031, 032, 033, 045, 046, 047. Consumers should check lot numbers and contact Dabur for details.
CGMP Deviations; deficiencies observed during FDA inspection
Dabur India Limited is recalling Med Pride hydrocortisone cream 1% tubes (1 oz) because FDA inspections found manufacturing deviations. This recall affects specific production lots that were made in India and sold in the U.S. through Shield Line LLC.
The FDA identified manufacturing deviations during an inspection, which means the product may not meet quality standards. However, the recall record does not specify what these deviations are or how they could cause harm in normal use.
People who own or use the recalled Med Pride hydrocortisone cream 1% tubes (1 oz) with lot numbers 001, 002, 013, 016, 031, 032, 033, 045, 046, or 047 are affected. Those using the product for medical purposes may be at risk if the manufacturing deviations impact safety.
Check the lot number on the tube, which should be one of 001, 002, 013, 016, 031, 032, 033, 045, 046, or 047. The product is labeled as Med Pride hydrocortisone cream 1% with a net weight of 1 ounce (28.3g).
Look for the lot number on the tube, which should be one of 001, 002, 013, 016, 031, 032, 033, 045, 046, or 047.
The FDA found manufacturing deviations during an inspection, but the specific deficiencies are not detailed in the recall notice.
Check the lot number on the tube, which should be one of 001, 002, 013, 016, 031, 032, 033, 045, 046, or 047.
The recall record does not specify a remedy, so contact Dabur India Limited directly for instructions.
We’ve drafted a message you can send Dabur to request your refund or repair — edit it as you like.
Subject: Recall D-0640-2026 — Dabur Dabur Hello, I own a Dabur that is covered by recall D-0640-2026 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.
