Dabur India Limited recalls Circle K triple antibiotic ointment due to FDA inspection findings of CGMP deviations. Affected lots from Cedar Rapids, IA. Consumers should check labels for lot numbers 0001 or 0005.
CGMP Deviations; deficiencies observed during FDA inspection
Dabur India Limited is recalling Circle K triple antibiotic ointment tubes from specific lots because of quality control issues found during an FDA inspection. This recall affects consumers who have these particular lot numbers and may pose risks if the product is used without proper quality assurance.
The FDA identified quality control deviations during an inspection of the manufacturing process. This means the product may not meet safety standards, though the exact nature of the deficiencies is not specified in the recall notice.
Anyone who purchased Circle K triple antibiotic ointment tubes with lot numbers 0001 or 0005 from Lil' Drug Store Products, Inc. in Cedar Rapids, IA. People using this ointment for skin care or minor wounds are most at risk due to potential quality issues.
Check the label for 'Circle K' triple antibiotic ointment with lot numbers 0001 or 0005. The product was manufactured for Lil' Drug Store Products, Inc. in Cedar Rapids, IA and sold with a net weight of 0.5 oz (14.2g).
Look for lot numbers 0001 or 0005 on the Circle K triple antibiotic ointment tube.
The FDA found quality control deviations during an inspection of the manufacturing process, but the specific deficiencies are not detailed in this recall notice.
The recall notice does not specify a remedy, so check the product label for lot numbers 0001 or 0005 and contact Dabur India Limited for further instructions.
The recall notice states that the product was found to have CGMP deviations during an FDA inspection, but it does not confirm if the product is unsafe for use.
We’ve drafted a message you can send Dabur to request your refund or repair — edit it as you like.
Subject: Recall D-0631-2026 — Dabur Dabur Hello, I own a Dabur that is covered by recall D-0631-2026 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.
