A-S Medication Solutions recalls metformin extended-release tablets (500mg, 180 tablets) due to foreign tablets present in some lots. Consumers should check product details and contact the company for guidance.
Presence of Foreign Tablets/Capsules.
A-S Medication Solutions has recalled metformin extended-release tablets (500mg, 180 tablets) because foreign tablets or capsules were found in some batches. This could lead to unintended medication intake if the foreign items are consumed.
Foreign tablets or capsules may be present in the medication, which could lead to unintended medication intake if consumed. This poses a low risk of harm as the foreign items are not expected to cause serious injury or death.
People who own or use metformin extended-release tablets (500mg, 180 tablets) packaged by A-S Medication Solutions in the U.S. are affected. Those with diabetes who take this medication are most at risk.
Check for the product name 'Metformin Hydrochloride Extended-Release 500mg, 180 tablets' and the lot number 4260340 on the packaging. The expiration date is December 31, 2025.
Look for the lot number 4260340 and expiration date of December 31, 2025 on the packaging.
The recall is due to foreign tablets or capsules being present, which could lead to unintended medication intake. However, the risk is low and does not cause serious injury.
Check for the lot number 4260340 and expiration date of December 31, 2025 on the packaging.
The recall does not specify a remedy, so contact A-S Medication Solutions for guidance.
We’ve drafted a message you can send A-S Medication Solutions to request your refund or repair — edit it as you like.
Subject: Recall D-0292-2025 — A-S Medication Solutions A-S Medication Solutions Hello, I own a A-S Medication Solutions that is covered by recall D-0292-2025 from A-S Medication Solutions. 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.
