US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jan 4, 2024 (3 years ago)

Fluocinolone Acetonide Oil, 0.01% (Ear Drops), package in 1 Oz. (20 mL fill volume)…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Failed Excipient Specifications: OOS for assay of Isopropyl Alcohol

What was recalled

Fluocinolone Acetonide Oil, 0.01% (Ear Drops), package in 1 Oz. (20 mL fill volume) bottle, Rx only, Manufactured by: Glenmark Pharmaceuticals Ltd., Village: Kishanpura, Baddi Nalagarh Road, District: Solan, Himachal Pradesh - 173205, India, Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430, NDC 68462-185-56

Recalling firm
Glenmark Pharmaceuticals Inc., USA
NDC code
68462-185-56
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0259-2024

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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