Harvard Drug Group recalls 100mg Gabapentin Capsules (NDC 55154-3363-0) with defective blister packaging that may not seal properly. Affected lots M05205A and M05205B expire 10/2026.
Defective container; blister packaging inadequately sealed.
Harvard Drug Group is recalling 100mg Gabapentin Capsules that have blister packaging which may not seal properly. This could lead to the capsules being exposed to moisture or contaminants, potentially affecting safety and effectiveness.
The blister packaging is inadequately sealed, which could allow moisture or contaminants to enter the capsules. This might affect the medication's stability and effectiveness, but does not pose an immediate risk of injury.
Prescription patients who received the recalled capsules from the specified lots and expiration dates. Those with specific medical conditions requiring precise dosing may be at slightly higher risk.
Check for the product name 'Gabapentin Capsules, USP, 100 mg, 10 capsules (10x1) per bag' on the packaging. Look for lot numbers M05205A or M05205B with an expiration date of 10/2026.
Look for lot numbers M05205A or M05205B on the packaging with an expiration date of 10/2026.
The recall is due to potential packaging issues that could affect medication stability, but the product is not unsafe to use if the packaging is intact.
Check for lot numbers M05205A or M05205B with an expiration date of 10/2026 on the packaging.
The recall does not specify a remedy, so contact your pharmacist or healthcare provider for guidance.
We’ve drafted a message you can send Harvard Drug Group to request your refund or repair — edit it as you like.
Subject: Recall D-0508-2025 — Harvard Drug Group Harvard Drug Group Hello, I own a Harvard Drug Group that is covered by recall D-0508-2025 from 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.
