The Harvard Drug Group recalls Carbidopa and Levodopa tablets due to blister packaging that may not seal properly. This could lead to medication exposure risks for patients using prescription medication.
Packaging defect: observed packaging defect, blister packaging inadequately sealed.
The Harvard Drug Group is recalling Carbidopa and Levodopa tablets (25 mg/100 mg) because the blister packaging may not seal properly. This defect could expose the medication to air or moisture, potentially affecting its safety and effectiveness for patients using these prescription drugs.
The blister packaging may not seal properly, which could allow the medication to be exposed to air or moisture. This might affect the medication's stability and effectiveness, but it does not pose an immediate risk of injury or serious harm.
Patients prescribed Carbidopa and Levodopa tablets by a doctor. Those using the medication for Parkinson's disease or other conditions are most at risk.
Check for the product name 'Carbidopa and Levodopa Tablets, USP 25 mg/100 mg', 10x10 Unit Dose carton, Rx Only. The lot number M04145 with an expiration date of January 2024.
Look for the lot number M04145 and expiration date of January 2024 on the packaging.
The recall is due to a packaging defect that may affect the medication's stability, but it does not pose an immediate risk of injury or serious harm.
Check for the product name 'Carbidopa and Levodopa Tablets, USP 25 mg/100 mg', 10x10 Unit Dose carton, Rx Only with lot number M04145 and expiration date January 2024.
The recall does not specify a remedy, so you should check with your doctor or pharmacist for guidance.
We’ve drafted a message you can send The Harvard Drug Group to request your refund or repair — edit it as you like.
Subject: Recall D-0432-2023 — The Harvard Drug Group The Harvard Drug Group Hello, I own a The Harvard Drug Group that is covered by recall D-0432-2023 from The Harvard Drug Group. 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.
