Morton Grove Pharmaceuticals, Inc. recalls Amoxicillin and Clavulanate Potassium for Oral Suspension, USP, 250/62.5 mg per 5 mL, 100 mL (when reconstituted)
Morton Grove Pharmaceuticals recalls Amoxicillin oral suspension due to customer reports of blue foreign material (nitrile glove) in product. Stop using immediately if you have this specific batch.
Lower-risk recall
Presence of Foreign Substance: customer complaint of blue foreign material identified as a portion of a nitrile glove was discovered in product.
Contact the company & request your remedy
What happened, in plain English
Morton Grove Pharmaceuticals is recalling Amoxicillin and Clavulanate Potassium oral suspension because customers reported finding blue foreign material, identified as a portion of a nitrile glove, in the product. This could pose a risk of ingestion of foreign material. Read more at govinfonow.com/recall/41403-morton-grove-amoxicillin-recall-blue-foreign-material-found.
Source Summary by GovInfoNow · govinfonow.com/recall/41403-morton-grove-amoxicillin-recall-blue-foreign-material-found · Updated October 7, 2026 · FDA enforcement record: FDA #D-1125-2017
Cite this page
“Morton Grove Amoxicillin Recall: Blue Foreign Material Found.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/41403-morton-grove-amoxicillin-recall-blue-foreign-material-found. Based on FDA recall #D-1125-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1125-2017%22&limit=1).
Why it’s dangerous
The hazard involves a small piece of blue foreign material (identified as a nitrile glove) being found in the product. This could be ingested by a child or patient, potentially causing harm from the foreign substance.
Who’s affected
People who have the specific Amoxicillin oral suspension bottle with NDC 60432-065-00 and batch number KH60276 (expiring 10/18) are affected. Children and infants are at higher risk due to potential ingestion of foreign material.
How to tell if you have this one
Look for the bottle labeled 'Amoxicillin and Clavulanate Potassium for Oral Suspension, USP, 250/62.5 mg per 5 mL, 100 mL (when reconstituted)' with NDC 60432-065-00 and batch number KH60276 (expiring 10/18).
- Brand
Morton Grove Pharmaceuticals- Category
Drug
What to do — step by step
Stop Using Immediately
Discard the product if you have the specific batch number KH60276 (expiring 10/18) as it contains foreign material.
Questions people ask
Why was this product recalled?
The recall was initiated after customer complaints of blue foreign material identified as a portion of a nitrile glove being found in the product.
Is this product safe to use?
No, the product contains foreign material that could be ingested, so it should be discarded immediately if you have the specific batch.
What should I do if I have this product?
Discard the product immediately and contact Morton Grove Pharmaceuticals for further instructions.
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-1125-2017 — Morton Grove Pharmaceuticals Morton Grove Pharmaceuticals Hello, I own a Morton Grove Pharmaceuticals that is covered by recall D-1125-2017 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-1125-2017 (August 10, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1125-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.