Teva Pharmaceuticals recalls Matzim LA 240mg extended-release tablets due to failed dissolution specifications. This may affect medication effectiveness. Check your product details to see if you need to take action.
Failed Dissolution Specifications: below specification limits for dissolution.
Teva Pharmaceuticals is recalling Matzim LA (Diltiazem Hydrochloride) 240mg extended-release tablets because they may not dissolve properly as intended. This could lead to inconsistent medication levels in the body, potentially affecting treatment effectiveness.
The tablets may not dissolve properly in the stomach, which could lead to inconsistent medication levels. This might cause the medication to not work as intended, potentially affecting heart condition treatment.
People with prescriptions for Matzim LA 240mg tablets who received this specific product from the manufacturer. Those with heart conditions requiring this medication are most at risk.
Check for the product name Matzim LA, 240mg, 30-count bottles, Rx Only. The lot number 1411596A and expiration date 09/22 are specific identifiers for this recall.
Look for the product name Matzim LA, 240mg, 30-count bottles, Rx Only with lot number 1411596A and expiration date 09/22.
The recall is for medication that may not dissolve properly, which could affect treatment effectiveness. However, it does not pose an immediate risk of serious injury.
Check for Matzim LA 240mg tablets with lot number 1411596A and expiration date 09/22.
The recall does not specify a remedy, so contact your healthcare provider for advice on whether to continue using the medication.
We’ve drafted a message you can send Teva Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-1303-2022 — Teva Pharmaceuticals Teva Pharmaceuticals Hello, I own a Teva Pharmaceuticals that is covered by recall D-1303-2022 from Teva 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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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.
