ACETAMINOPHEN REGULAR-STRENGTH PAIN RELIEVER tablets, 325 mg, 100-count bottle, Distributed by Medline Industries, Inc., Mundelein, ILL 60060, NDC 53329-642-30.
Reported: February 24, 2016 Initiated: September 25, 2015 #D-0663-2016
Product Description
ACETAMINOPHEN REGULAR-STRENGTH PAIN RELIEVER tablets, 325 mg, 100-count bottle, Distributed by Medline Industries, Inc., Mundelein, ILL 60060, NDC 53329-642-30.
Reason for Recall
Labeling: Label Error on Declared Strength- Bottles containing 500 mg acetaminophen tablets mislabeled to contain 325 mg tablets.
Details
- Recalling Firm
- Medline Industries Inc
- Distribution
- Nationwide
- Location
- Mundelein, IL
Frequently Asked Questions
What product was recalled? ▼
ACETAMINOPHEN REGULAR-STRENGTH PAIN RELIEVER tablets, 325 mg, 100-count bottle, Distributed by Medline Industries, Inc., Mundelein, ILL 60060, NDC 53329-642-30.. Recalled by Medline Industries Inc.
Why was this product recalled? ▼
Labeling: Label Error on Declared Strength- Bottles containing 500 mg acetaminophen tablets mislabeled to contain 325 mg tablets.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 24, 2016. Severity: Critical. Recall number: D-0663-2016.
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