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Drug recall · FDA · Published November 17, 2017

Lupin Limited recalls Pravastatin Sodium USP, tablets, 40 mg, 90-count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc.,

Presence of foreign tablets/capsules: This product lot is being recalled due to a pharmacy complaint where one Duloxetine Delayed Release Capsule, 30mg was found in a Pravastatin Sodium Tablets USP, 40mg bottle.

🇺🇸 FDA recall #D-0092-2018DrugLupin Limited ›
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Recalling firmLupin Limited15 - B I Phase 1a, I D C Verna Industrial Road · Vasco Da Gama, N/A N/A
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
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Source Page by GovInfoNow · govinfonow.com/recall/41048-lupin-limited-recalls-pravastatin-sodium-usp-tablets-40-mg-90 · Recall date November 17, 2017 · FDA enforcement record: FDA #D-0092-2018

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“Lupin Limited recalls Pravastatin Sodium USP, tablets, 40 mg, 90-count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc.,.” GovInfoNow, recall dated November 17, 2017. https://govinfonow.com/recall/41048-lupin-limited-recalls-pravastatin-sodium-usp-tablets-40-mg-90. Based on FDA recall #D-0092-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0092-2018%22&limit=1).

How to tell if you have this one

  • Brand
    Lupin Limited
  • Category
    Drug
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Contact Lupin Limited

We’ve drafted a message you can send Lupin Limited to request your refund or repair — edit it as you like.

Subject: Recall D-0092-2018 — Lupin Limited Lupin Limited recalls Pravastatin Sodium USP, tablets, 40 mg, 90-count bottle, Rx onl

Hello,

I own a Lupin Limited recalls Pravastatin Sodium USP, tablets, 40 mg, 90-count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., that is covered by recall D-0092-2018 from Lupin Limited.

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-0092-2018 (November 17, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0092-2018 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA