FDASeptember 25, 2015drug

ACETAMINOPHEN REGULAR-STRENGTH PAIN RELIEVER tablets, 325 mg, 100-count bottle, Distributed by Medline Industries, Inc., Mundelein, ILL 60060, NDC 53329-642-30.

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

The hazard

Labeling: Label Error on Declared Strength- Bottles containing 500 mg acetaminophen tablets mislabeled to contain 325 mg tablets.

What to do

FDA enforcement status: Terminated

Brands named

medline

Recall history

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

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