Teva Pharmaceuticals USA recalls Amoxicillin for Oral Suspension USP, 125 mg per 5 mL, packaged in (a) 150 mL bottle (NDC 0093-4150-80) (b) 80 mL bottle
Teva Pharmaceuticals USA recalls Amoxicillin oral suspension (125mg/5mL) with low amoxicillin content. This may not treat infections effectively. Products sold in Canada with specific NDC numbers and expiration dates are affected.
Lower-risk recall
Subpotent Product: assay results for Amoxicillin were below the specification limits.
Contact the company & request your remedy
What happened, in plain English
Teva Pharmaceuticals USA is recalling Amoxicillin oral suspension products that contain less amoxicillin than specified. This means the medication may not work as intended to treat infections, potentially leading to ineffective treatment. Read more at govinfonow.com/recall/38911-teva-recalls-amoxicillin-oral-suspension-due-to-subpotent-product.
Source Summary by GovInfoNow · govinfonow.com/recall/38911-teva-recalls-amoxicillin-oral-suspension-due-to-subpotent-product · Updated October 5, 2026 · FDA enforcement record: FDA #D-1205-2019
Cite this page
“Teva Recalls Amoxicillin Oral Suspension Due to Subpotent Product.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/38911-teva-recalls-amoxicillin-oral-suspension-due-to-subpotent-product. Based on FDA recall #D-1205-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1205-2019%22&limit=1).
Why it’s dangerous
The recalled Amoxicillin products have lower-than-stated amoxicillin content. This means the medication may not be strong enough to treat infections effectively. The product is still safe to use but may not work as intended.
Who’s affected
People who have been prescribed this medication by a doctor and are using the recalled Amoxicillin oral suspension products. Those with infections requiring treatment may be at risk of ineffective therapy.
How to tell if you have this one
Check for the product name 'Amoxicillin for Oral Suspension USP, 125 mg per 5 mL'. Look for NDC numbers 0093-4150-80 (150 mL bottle) or 0093-4150-79 (80 mL bottle). Products manufactured in Canada with specific expiration dates are affected.
- Brand
Teva- Category
Drug
What to do — step by step
Check Product Details
Verify the NDC numbers and expiration dates listed in the recall notice to confirm if your product is affected.
Questions people ask
Is this product safe to use?
Yes, the product is safe but may not be effective due to lower-than-stated amoxicillin content.
What should I do if I have this product?
Check the NDC numbers and expiration dates to see if your product is affected. If it is, contact your doctor for alternative treatment options.
How can I tell if my product is recalled?
Look for NDC numbers 0093-4150-80 (150 mL bottle) or 0093-4150-79 (80 mL bottle) with specific expiration dates listed in the recall notice.
Contact Teva
We’ve drafted a message you can send Teva to request your refund or repair — edit it as you like.
Subject: Recall D-1205-2019 — Teva Teva Hello, I own a Teva that is covered by recall D-1205-2019 from Teva. 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-1205-2019 (April 12, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1205-2019 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.