International Laboratories, Inc. recalls Pravastatin Sodium Tablets, USP, 40 mg, 30-count bottle, Rx only, Packaged for: International Laboratories, LLC. St.
Labeling: Label mix-up, the product labeled as Pravastatin sodium tablets 40 mg was filled with Bupropion hydrochloride XL Tablets 300 mg.
Recall notice
Labeling: Label mix-up, the product labeled as Pravastatin sodium tablets 40 mg was filled with Bupropion hydrochloride XL Tablets 300 mg.
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Source Page by GovInfoNow · govinfonow.com/recall/41408-international-laboratories-inc-recalls-pravastatin-sodium-tablets-usp-40-mg · Recall date August 7, 2017 · FDA enforcement record: FDA #D-0102-2018
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“International Laboratories, Inc. recalls Pravastatin Sodium Tablets, USP, 40 mg, 30-count bottle, Rx only, Packaged for: International Laboratories, LLC. St..” GovInfoNow, recall dated August 7, 2017. https://govinfonow.com/recall/41408-international-laboratories-inc-recalls-pravastatin-sodium-tablets-usp-40-mg. Based on FDA recall #D-0102-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0102-2018%22&limit=1).
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We’ve drafted a message you can send International Laboratories, Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-0102-2018 — International Laboratories, Inc. International Laboratories, Inc. recalls Pravastatin Sodium Tablet Hello, I own a International Laboratories, Inc. recalls Pravastatin Sodium Tablets, USP, 40 mg, 30-count bottle, Rx only, Packaged for: International Laboratories, LLC. St. that is covered by recall D-0102-2018 from International Laboratories, 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-0102-2018 (August 7, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0102-2018 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.