RemedyRepack Inc. recalls Nitrofurantoin Monohydrate/Macrocrystals capsules,100 mg, packaged in HDPE 60 cc bottles, Rx only, MFG: Sandoz Inc.,
RemedyRepack recalls Nitrofurantoin 100mg capsules due to potential cross contamination with unrelated drugs like Benazepril and Haloperidol. Consumers should contact the company for details.
Lower-risk recall
Cross contamination with other products: Product is being recalled due to the potential presence of unrelated ingredients (Benazepril, Haloperidol and Perphenazine).
Contact the company & request your remedy
What happened, in plain English
RemedyRepack is recalling Nitrofurantoin Monohydrate/Macrocrystals capsules that may contain unrelated ingredients such as Benazepril and Haloperidol. This cross-contamination risk could lead to unintended medication interactions or adverse effects. Read more at govinfonow.com/recall/39437-remedyrepack-nitrofurantoin-capsules-recall-cross-contamination-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/39437-remedyrepack-nitrofurantoin-capsules-recall-cross-contamination-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-0284-2019
Cite this page
“RemedyRepack Nitrofurantoin Capsules Recall: Cross Contamination Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/39437-remedyrepack-nitrofurantoin-capsules-recall-cross-contamination-risk. Based on FDA recall #D-0284-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0284-2019%22&limit=1).
Why it’s dangerous
The capsules may contain unrelated medications like Benazepril and Haloperidol due to cross-contamination during repackaging. This could cause unintended medication interactions or adverse effects if taken without proper medical guidance.
Who’s affected
People who have been prescribed Nitrofurantoin capsules by a doctor and received the recalled product. Those with specific medical conditions or taking other medications may be at higher risk.
How to tell if you have this one
Check for the product name 'Nitrofurantoin Monohydrate/Macrocrystals capsules, 100 mg' in HDPE 60 cc bottles. Look for lot numbers B0484872-081718, B0481339-081018, B0506246-092718, or B0509938-100418 with expiration dates up to 10/2019.
- Brand
RemedyRepack- Category
Drug
What to do — step by step
Check Product Details
Identify the lot number and expiration date on the packaging to confirm if the product is recalled.
Contact RemedyRepack
Reach out to RemedyRepack for specific instructions on how to return or dispose of the product.
Questions people ask
Why is this product being recalled?
The product may contain unrelated medications like Benazepril and Haloperidol due to cross-contamination during repackaging.
How can I tell if I have the recalled product?
Check for the product name 'Nitrofurantoin Monohydrate/Macrocrystals capsules, 100 mg' in HDPE 60 cc bottles with lot numbers B0484872-081718, B0481339-081018, B0506246-092718, or B0509938-100418.
What should I do if I have the recalled product?
Contact RemedyRepack for instructions on returning or disposing of the product.
Contact RemedyRepack
We’ve drafted a message you can send RemedyRepack to request your refund or repair — edit it as you like.
Subject: Recall D-0284-2019 — RemedyRepack RemedyRepack Hello, I own a RemedyRepack that is covered by recall D-0284-2019 from RemedyRepack. 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-0284-2019 (November 7, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0284-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- 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.