Class III

Drug Recall: Acetaminophen, USP 500mg, Pain Reliever/Fever Reducer, Extra Strength, Rapid Release Gelcaps, packaged in a 225-count HDPE bottle, further packaged in a carton, Distributed by Walgreen Co., 200 Wilmot

Granules Consumer Health Inc. · July 18, 2024

Reason for Recall

Label mix-up: Carton incorrectly labeled.

Product Description

Acetaminophen, USP 500mg, Pain Reliever/Fever Reducer, Extra Strength, Rapid Release Gelcaps, packaged in a 225-count HDPE bottle, further packaged in a carton, Distributed by Walgreen Co., 200 Wilmot Rd, Deerfield, IL 60015, Made in India

Distribution

Recalled lot was distributed to one distributor in IL who may have further distributed the product to the retail level.

States Affected

IL, IN

Quantity Affected

21,192 Bottles

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0627-2024

Status: terminated

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.