Teva Pharmaceuticals recalls specific amoxicillin-clavulanate oral suspension due to subpotent clavulanate potassium. This may result in ineffective treatment for bacterial infections. Consumers should contact the manufacturer for details.
Subpotent drug; Clavulanate Potassium component
Teva Pharmaceuticals is recalling a specific amoxicillin and clavulanate potassium oral suspension because it contains less clavulanate potassium than it should. This means the medication may not work effectively for bacterial infections, potentially leading to treatment failure.
The suspension contains less clavulanate potassium than it should, making it subpotent. This means the medication may not work effectively for bacterial infections, potentially leading to treatment failure if used without proper dosing.
Prescription holders of the specific amoxicillin-clavulanate suspension with NDC 0093-2277-7 manufactured in Canada by Teva Canada Limited. Patients on this medication for bacterial infections are most at risk.
Check for the product name 'Amoxicillin and Clavulanate Potassium for Oral Suspension USP, 200 mg/28.5 mg per 5mL, 100 mL (when reconstituted), Rx only'. Look for the NDC code 0093-2277-7 and lot number 100062316.
Reach out to Teva Pharmaceuticals USA, Inc. for specific instructions on handling the recalled product.
The recall indicates the medication may be subpotent, meaning it could be less effective than intended. Do not use without consulting the manufacturer.
Contact Teva Pharmaceuticals USA, Inc. for specific instructions on handling the recalled product.
Check for the NDC code 0093-2277-7 and lot number 100062316 on the product label.
We’ve drafted a message you can send Teva to request your refund or repair — edit it as you like.
Subject: Recall D-0151-2026 — Teva Teva Hello, I own a Teva that is covered by recall D-0151-2026 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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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.
