Medline Industries Inc recalls ACETAMINOPHEN REGULAR-STRENGTH PAIN RELIEVER tablets, 325 mg, 100-count bottle, Distributed by Medline Industries,
Labeling: Label Error on Declared Strength- Bottles containing 500 mg acetaminophen tablets mislabeled to contain 325 mg tablets.
Recall notice
Labeling: Label Error on Declared Strength- Bottles containing 500 mg acetaminophen tablets mislabeled to contain 325 mg tablets.
Contact the company & request your remedy
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Source Page by GovInfoNow · govinfonow.com/recall/43614-medline-industries-inc-recalls-acetaminophen-regular-strength-pain-reliever-tablets · Recall date September 25, 2015 · FDA enforcement record: FDA #D-0663-2016
Cite this page
“Medline Industries Inc recalls ACETAMINOPHEN REGULAR-STRENGTH PAIN RELIEVER tablets, 325 mg, 100-count bottle, Distributed by Medline Industries,.” GovInfoNow, recall dated September 25, 2015. https://govinfonow.com/recall/43614-medline-industries-inc-recalls-acetaminophen-regular-strength-pain-reliever-tablets. Based on FDA recall #D-0663-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0663-2016%22&limit=1).
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- Brand
Medline Industries Inc- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Terminated- Distribution
Nationwide
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0662-2016 | ACETAMINOPHEN EXTRA-STRENGTH PAIN RELIEVER tablets, 500 mg, 100-count bottle, Distributed by Medline Industries, Inc., Mundelein, ILL 60060, NDC 53329-641-30.; lot # 45810; Exp. 05/18 | 7,372 HDPE Bottles |
| 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.; lot # 45810; Exp. 05/18 | — |
Contact Medline Industries Inc
We’ve drafted a message you can send Medline Industries Inc to request your refund or repair — edit it as you like.
Subject: Recall D-0663-2016 — Medline Industries Inc Medline Industries Inc recalls ACETAMINOPHEN REGULAR-STRENGTH PAIN RELIEVER Hello, I own a Medline Industries Inc recalls ACETAMINOPHEN REGULAR-STRENGTH PAIN RELIEVER tablets, 325 mg, 100-count bottle, Distributed by Medline Industries, that is covered by recall D-0663-2016 from Medline Industries Inc. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0663-2016 (September 25, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0663-2016 to see it in context.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.