SCA Pharmaceuticals, Inc. recalls Furosemide 100 mg added to 0.9% Sodium Chloride 100 mL Injection, 100 mL Single Dose Container bag, Rx Only, SCA
SCA Pharmaceuticals recalls Furosemide 100 mg injection with visible precipitate. This may affect drug effectiveness. Check product lot numbers for affected batches.
Lower-risk recall
Presence of Precipitate: Customer complaint for visible precipitate in product believed to be the active ingredient furosemide.
Contact the company & request your remedy
What happened, in plain English
SCA Pharmaceuticals is recalling Furosemide 100 mg injection due to visible precipitate in some batches. This could mean the medication isn't working properly. Affected products were sold with specific lot numbers and expiration dates. Read more at govinfonow.com/recall/39676-sca-furosemide-injection-recall-visible-precipitate-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/39676-sca-furosemide-injection-recall-visible-precipitate-risk · Updated October 6, 2026 · FDA enforcement record: FDA #D-1189-2018
Cite this page
“SCA Furosemide Injection Recall: Visible Precipitate Risk.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/39676-sca-furosemide-injection-recall-visible-precipitate-risk. Based on FDA recall #D-1189-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1189-2018%22&limit=1).
Why it’s dangerous
The product contains visible precipitate, which may indicate the active ingredient furosemide has separated. This could reduce the medication's effectiveness. The hazard is not described as causing injury or serious harm.
Who’s affected
People prescribed this medication by a doctor are likely affected. Those using the product without medical supervision are not at risk.
How to tell if you have this one
Check the product label for lot numbers: 20180711@18, 20180712@19, 20180712@21, 20180712@24, 20180713@19, 20180727@21, or 20180803@20. The expiration date is listed on the product.
- Brand
SCA- Product
Furosemide 100 mg added to 0.9% Sodium Chloride 100 mL Injection, 100 mL Single Dose Container bag, Rx Only, SCA- Category
Drug
What to do — step by step
Check Product Label
Look for lot numbers matching those listed in the recall notice.
Questions people ask
Is this product dangerous?
The recall is due to visible precipitate, which may affect the medication's effectiveness but does not cause injury or serious harm.
How do I know if I have the recalled product?
Check the product label for lot numbers: 20180711@18, 20180712@19, 20180712@21, 20180712@24, 20180713@19, 20180727@21, or 20180803@20.
What should I do if I have the recalled product?
The recall does not require immediate action. Check the product label and contact your doctor if you have concerns.
Contact SCA
We’ve drafted a message you can send SCA to request your refund or repair — edit it as you like.
Subject: Recall D-1189-2018 — SCA Furosemide 100 mg added to 0.9% Sodium Chloride 100 mL Injection, 100 mL Single Dose Container Hello, I own a Furosemide 100 mg added to 0.9% Sodium Chloride 100 mL Injection, 100 mL Single Dose Container bag, Rx Only, SCA that is covered by recall D-1189-2018 from SCA. 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-1189-2018 (August 27, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1189-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 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.