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Drug recall · FDA · Published December 22, 2016

Roxane Laboratories, Inc. recalls Furosemide Tablets USP, 20 mg, 1000 count bottles, Rx only, Roxane Laboratories, Inc., Columbus, Ohio 43216, NDC

Failed Tablet/Capsule Specifications: An unusually thick tablet was reported through a complaint.

🇺🇸 FDA recall #D-0437-2017DrugRoxane Laboratories, Inc. ›
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Recalling firmRoxane Laboratories, Inc.1809 Wilson Rd, N/A · Columbus, OH 43228-9579
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/42110-roxane-laboratories-inc-recalls-furosemide-tablets-usp-20-mg-1000 · Recall date December 22, 2016 · FDA enforcement record: FDA #D-0437-2017

Cite this page

“Roxane Laboratories, Inc. recalls Furosemide Tablets USP, 20 mg, 1000 count bottles, Rx only, Roxane Laboratories, Inc., Columbus, Ohio 43216, NDC.” GovInfoNow, recall dated December 22, 2016. https://govinfonow.com/recall/42110-roxane-laboratories-inc-recalls-furosemide-tablets-usp-20-mg-1000. Based on FDA recall #D-0437-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0437-2017%22&limit=1).

How to tell if you have this one

  • Brand
    Roxane Laboratories, Inc.
  • Category
    Drug
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Contact Roxane Laboratories, Inc.

We’ve drafted a message you can send Roxane Laboratories, Inc. to request your refund or repair — edit it as you like.

Subject: Recall D-0437-2017 — Roxane Laboratories, Inc. Roxane Laboratories, Inc. recalls Furosemide Tablets USP, 20 mg, 1000 cou

Hello,

I own a Roxane Laboratories, Inc. recalls Furosemide Tablets USP, 20 mg, 1000 count bottles, Rx only, Roxane Laboratories, Inc., Columbus, Ohio 43216, NDC that is covered by recall D-0437-2017 from Roxane 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-0437-2017 (December 22, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0437-2017 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