Harvard Drug Group recalls 600mg Gabapentin tablets (NDC 0904-6823-61) after finding a foreign tablet in some products. This recall is for prescription-only items sold between specific dates.
Product mixup: one foreign tablet found in product.
The Harvard Drug Group is recalling prescription 600mg Gabapentin tablets that may contain a foreign tablet. This mixup could lead to unintended medication intake if someone takes the foreign tablet instead of the intended medication.
The product contains a foreign tablet that could be taken by mistake, potentially causing unintended medication intake. This mixup occurs during manufacturing and distribution, but the risk is low since the foreign tablet is not a dangerous substance.
Prescription holders of the 600mg Gabapentin tablets with the specific NDC number and lot code. People who take these medications regularly are most at risk if they accidentally consume the foreign tablet.
Check for the NDC code 0904-6823-61 and lot number T04468 on the packaging. The product is a prescription-only 600mg Gabapentin tablet in cartons of 100 tablets.
Look for the NDC code 0904-6823-61 and lot number T04468 on the packaging to confirm if your product is affected.
The recall is for a foreign tablet mixup, not a dangerous substance. The risk is low as the foreign tablet is not intended for use.
Check for the NDC code 0904-6823-61 and lot number T04468 on the packaging. The product is a prescription-only 600mg Gabapentin tablet in cartons of 100 tablets.
No, but you should check your packaging for the NDC code and lot number to confirm if your product is affected.
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-0570-2023 — The Harvard Drug Group The Harvard Drug Group Hello, I own a The Harvard Drug Group that is covered by recall D-0570-2023 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.
