Sciegen Pharmaceuticals recalls 600mg Gabapentin tablets due to foreign 800mg tablets found in some bottles. Affected lots may contain incorrect strength.
Presence of Foreign Tablets/Capsules: Pharmacist reported presence of some Gabapentin tablets 800 mg comingled in Gabapentin 600 mg 500 count bottles.
Sciegen Pharmaceuticals is recalling Gabapentin 600mg tablets after a pharmacist reported some bottles contained 800mg tablets by mistake. This could lead to incorrect dosing if taken.
The recall involves 800mg Gabapentin tablets mistakenly mixed into 600mg bottles. Taking these could cause incorrect dosing, potentially leading to adverse effects. However, the risk is low as the tablets are only present in some bottles and not all patients are affected.
Prescription patients who received the recalled 600mg Gabapentin tablets. Those with specific medical conditions requiring precise dosing are at higher risk.
Check for the lot number G177092 on the bottle. The product is a 600mg Gabapentin tablet bottle with 500 tablets, manufactured in Hauppauge, NY, and expires November 2024.
Look for the lot number G177092 on the bottle. If present, the product is part of the recall.
A pharmacist reported that some bottles contained 800mg Gabapentin tablets by mistake, which could lead to incorrect dosing.
Check for the lot number G177092 on the bottle. The product is a 600mg Gabapentin tablet bottle with 500 tablets, manufactured in Hauppauge, NY, and expires November 2024.
The recall does not specify a remedy, so contact your pharmacist or healthcare provider for advice.
We’ve drafted a message you can send Sciegen Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0354-2023 — Sciegen Pharmaceuticals Sciegen Pharmaceuticals Hello, I own a Sciegen Pharmaceuticals that is covered by recall D-0354-2023 from Sciegen 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
