US Drug Recall Register
Class II · Moderate risk Terminated Initiated Oct 5, 2018 (8 years ago)

Fluocinolone Acetonide Topical Solution, USP 0.01%, 60ml Bottle, Manufactured for: Lupin…

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

Why it was recalled

Failed Impurities/Degradation Specifications:Out of specification result noticed for total impurities observed during stability analysis

What was recalled

Fluocinolone Acetonide Topical Solution, USP 0.01%, 60ml Bottle, Manufactured for: Lupin Pharmaceutical, Inc. Baltimore, MD 21202 Manufactured by: Novel Laboratories, Inc. Somerset, NJ 08873. NDC 43386-069-60

Recalling firm
Lupin Somerset
NDC code
43386-069-60
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0092-2019

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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