FDADecember 16, 2019drug

Hydrocortisone and Acetic Acid Otic Solution, USP, 10 mL dropper bottle, Rx only, HI-TECH PHARMACAL CO., INC., Amityville, NY 11701; NDC 50383-901-10.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Subpotent Drug: Low Out of specification (OOS) assay results for the hydrocortisone portion of this product.

What to do

FDA enforcement status: Terminated

Brands named

akorn

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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