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Drug recall · FDA · Published June 28, 2018

LUPIN SOMERSET recalls Nitrofurantoin Oral Suspension USP, 25mg/5mL, 230 mL Bottle, Rx Only, Manufactured by: Novel Laboratories, Inc.

Subpotent Drug and Failed Content Uniformity.

🇺🇸 FDA recall #D-0927-2018DrugLUPIN SOMERSET ›
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Contact the company & request your remedy

Recalling firmLUPIN SOMERSET400 Campus Dr · Somerset, NJ 08873-1145
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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We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.

Source Page by GovInfoNow · govinfonow.com/recall/40392-lupin-somerset-recalls-nitrofurantoin-oral-suspension-usp-25mg-5ml-230 · Recall date June 28, 2018 · FDA enforcement record: FDA #D-0927-2018

Cite this page

“LUPIN SOMERSET recalls Nitrofurantoin Oral Suspension USP, 25mg/5mL, 230 mL Bottle, Rx Only, Manufactured by: Novel Laboratories, Inc..” GovInfoNow, recall dated June 28, 2018. https://govinfonow.com/recall/40392-lupin-somerset-recalls-nitrofurantoin-oral-suspension-usp-25mg-5ml-230. Based on FDA recall #D-0927-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0927-2018%22&limit=1).

How to tell if you have this one

  • Brand
    LUPIN SOMERSET
  • Product
    Nitrofurantoin Oral Suspension USP, 25mg/5mL, 230 mL Bottle, Rx Only, Manufactured by: Novel Laboratories, Inc.
  • Category
    Drug
Take action

Contact LUPIN SOMERSET

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

Subject: Recall D-0927-2018 — LUPIN SOMERSET Nitrofurantoin Oral Suspension USP, 25mg/5mL, 230 mL Bottle, Rx Only, Manufactured b

Hello,

I own a Nitrofurantoin Oral Suspension USP, 25mg/5mL, 230 mL Bottle, Rx Only, Manufactured by: Novel Laboratories, Inc. that is covered by recall D-0927-2018 from LUPIN SOMERSET.

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-0927-2018 (June 28, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0927-2018 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