Medline Industries Inc recalls ACETAMINOPHEN REGULAR-STRENGTH PAIN RELIEVER tablets, 325 mg, 100-count bottle, Distributed by Medline Industries, Inc.,

Recalled February 24, 2016 · FDA recall D-0663-2016 · Medline Industries

Hazard

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

Sold at

Nationwide

Description

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

Product

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

Manufacturer(s)

Medline Industries Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →