Morton Grove Pharmaceuticals, Inc. recalls Prednisolone Sodium Phosphate Oral Solution, 15 mg/5 mL, 8 fl oz (237 mL) Bottle, Rx only, Manufactured By: Morton
Morton Grove Pharmaceuticals recalls Prednisolone Sodium Phosphate Oral Solution due to potential tamper-evident foil seal failure. This may allow unauthorized access to the medication. Affected products have NDC 60432-212-08 and lot US1259.
Lower-risk recall
Defective Container: Tamper Evident foil seal not completely intact.
Contact the company & request your remedy
What happened, in plain English
Morton Grove Pharmaceuticals is recalling Prednisolone Sodium Phosphate Oral Solution bottles because the tamper-evident foil seal might not be fully intact. This could allow someone to access the medication without the user noticing, which is a safety concern for people taking prescription steroids. Read more at govinfonow.com/recall/39863-morton-grove-pharmaceuticals-prednisolone-oral-solution-recall-defective-container-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/39863-morton-grove-pharmaceuticals-prednisolone-oral-solution-recall-defective-container-risk · Updated October 6, 2026 · FDA enforcement record: FDA #D-1042-2018
Cite this page
“Morton Grove Pharmaceuticals Prednisolone Oral Solution Recall: Defective Container Risk.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/39863-morton-grove-pharmaceuticals-prednisolone-oral-solution-recall-defective-container-risk. Based on FDA recall #D-1042-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1042-2018%22&limit=1).
Why it’s dangerous
The tamper-evident foil seal on the bottle may not be completely intact, which could allow unauthorized access to the medication. This means someone might be able to open the bottle without the user noticing, potentially leading to accidental misuse or contamination of the medication.
Who’s affected
People with a prescription for Prednisolone Sodium Phosphate Oral Solution who received this specific bottle size and lot number. Those who are most at risk are individuals taking the medication for conditions like autoimmune disorders or chronic inflammation.
How to tell if you have this one
Check for the bottle labeled 'Prednisolone Sodium Phosphate Oral Solution, 15 mg/5 mL, 8 fl oz (237 mL)' with NDC 60432-212-08 and lot number US1259. This product was manufactured by Morton Grove Pharmaceuticals in Morton Grove, IL.
- Brand
Morton Grove Pharmaceuticals- Category
Drug
What to do — step by step
Check Product Details
Look for the NDC code 60432-212-08 and lot number US1259 on the bottle label.
Questions people ask
Is this product safe to use?
The recall is due to a potential issue with the tamper-evident seal, but the product is still safe to use if the seal appears intact. However, the manufacturer recommends checking the seal and following the recall instructions.
How can I tell if I have the recalled product?
Check for the NDC code 60432-212-08 and lot number US1259 on the bottle label. This product was manufactured by Morton Grove Pharmaceuticals in Morton Grove, IL.
What should I do if I have the recalled product?
The recall does not specify a remedy, so you should check the product details and contact your healthcare provider for guidance.
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-1042-2018 — Morton Grove Pharmaceuticals Morton Grove Pharmaceuticals Hello, I own a Morton Grove Pharmaceuticals that is covered by recall D-1042-2018 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-1042-2018 (July 24, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1042-2018 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.