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Drug recall · FDA · Published September 23, 2019

Morton Grove Pharmaceuticals, Inc. recalls Prednisolone Sodium Phosphate Oral Solution, 15 mg/5 mL, packaged in a 8 fl oz (237 mL) bottle, Rx only, Manufactured

Morton Grove Pharmaceuticals recalls Prednisolone Sodium Phosphate Oral Solution due to failed impurity specifications. This medication, sold Rx only, may contain harmful impurities that could affect safety.

🇺🇸 FDA recall #D-0130-2020DrugMorton Grove Pharmaceuticals ›
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Contact the company & request your remedy

Recalling firmMorton Grove Pharmaceuticals, Inc.6451 Main St, N/A · Morton Grove, IL 60053-2633
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.
✎ GovInfoNow plain-language explainer

What happened, in plain English

Morton Grove Pharmaceuticals is recalling Prednisolone Sodium Phosphate Oral Solution (15 mg/5 mL) because it failed impurity testing. This could pose a risk to users, especially those taking the medication as prescribed. Read more at govinfonow.com/recall/37914-morton-grove-pharmaceuticals-prednisolone-oral-solution-recall-impurity-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/37914-morton-grove-pharmaceuticals-prednisolone-oral-solution-recall-impurity-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-0130-2020

Cite this page

“Morton Grove Pharmaceuticals Prednisolone Oral Solution Recall: Impurity Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37914-morton-grove-pharmaceuticals-prednisolone-oral-solution-recall-impurity-risk. Based on FDA recall #D-0130-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0130-2020%22&limit=1).

Why it’s dangerous

The medication failed impurity testing, meaning it may contain harmful substances that could affect safety. This is a quality issue that could lead to potential health risks if the impurities are not properly controlled.

Who’s affected

People who have been prescribed this medication by a doctor and use it as directed. Those with specific health conditions requiring this medication may be at higher risk.

How to tell if you have this one

Check for the product name 'Prednisolone Sodium Phosphate Oral Solution', 15 mg/5 mL, in an 8 fl oz bottle. The NDC code is 60432-212-08 with specific lot numbers and expiration dates listed in the recall notice.

  • Brand
    Morton Grove Pharmaceuticals
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the NDC code 60432-212-08 and lot numbers US1450, US1570, UT1018, UT1173, UT1348, UT1354 with specific expiration dates.

✎ GovInfoNow

Questions people ask

Is this medication safe to use?

The recall indicates the medication failed impurity specifications, so it is not safe to use as recalled. Consult your doctor for guidance.

What should I do if I have this medication?

The recall does not specify a remedy, so contact your doctor or pharmacist for advice on whether to stop using it.

How can I check if my medication is recalled?

Check the NDC code 60432-212-08 and lot numbers listed in the recall notice to determine if your medication is affected.

Take action

Contact Morton Grove Pharmaceuticals

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

Subject: Recall D-0130-2020 — Morton Grove Pharmaceuticals Morton Grove Pharmaceuticals

Hello,

I own a Morton Grove Pharmaceuticals that is covered by recall D-0130-2020 from Morton Grove Pharmaceuticals.

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-0130-2020 (September 23, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0130-2020 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.
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