FDA · Drugs · Wednesday, June 24

Rapidol recall

Dabur India Limited recalled Rapidol on June 24, 2026 because of cGMP Deviations; deficiencies observed during FDA inspection. It was sold nationwide.

Why it was recalled

CGMP Deviations; deficiencies observed during FDA inspection

What's recalled

Rapidol, Triple Antibiotic First Aid Ointment, Bacitracin Zinc 400 units, Neomycin Sulfate 3.5 mg, Polymyxin-B Sulfate 5,000 units, net wt. 2oz (57g) tubes, Distributed by/por: Pharmadel LLC, New Castle, DE 19720, Made in India, UPC 8 10096 77162 9.

Quantity: 84 tubes

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company: Dabur India Limited, Dadra And Nagar Haveli
Date: Wednesday, June 24
Severity: Class II
the product could cause temporary or reversible health problems.
Where sold: Nationwide
US Nationwide.
Status: Ongoing
Recall number: D-0633-2026
Source: U.S. Food and Drug Administration

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