FDAFDA · Food and drugs·Recall number D-0663-2016
ACETAMINOPHEN REGULAR-STRENGTH PAIN RELIEVER tablets, 325 mg, 100-count bottle, Distributed by Medline Industries, Inc., Mundelein, ILL 60060, NDC 53329-642-30.
Published February 24, 2016 · Recall initiated: September 25, 2015
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Labeling: Label Error on Declared Strength- Bottles containing 500 mg acetaminophen tablets mislabeled to contain 325 mg tablets.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Medline Industries Inc
- Distributor
- Nationwide
- Lot
- lot # 45810; Exp. 05/18
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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