Harvard Drug Group recalls 100mg Gabapentin Capsules (100-count blister packs) because the packaging may not seal properly. This could lead to contamination or exposure to air. Consumers should contact the manufacturer for details.
Defective container; blister packaging inadequately sealed.
Harvard Drug Group is recalling 100mg Gabapentin Capsules (100-count blister packs) because the blister packaging may not seal properly. This could allow contamination or exposure to air, though serious injury is not expected.
The blister packaging may not seal properly, which could allow contamination or exposure to air. This might lead to the medication becoming ineffective or causing unintended reactions, but serious injury is not expected.
People who have the 100mg Gabapentin Capsules (100-count blister packs) from Harvard Drug Group. Those with prescription medication for seizures or nerve pain are most at risk.
Check for the product name 'Gabapentin Capsules, USP, 100 mg, 100 capsules (10x10)' in blister pack cartons. The lot number is M05205 with an expiration date of 10/2026.
Look for the lot number M05205 and expiration date 10/2026 on the blister pack carton.
The product may not seal properly, which could lead to contamination or exposure to air, but serious injury is not expected.
Check for the product name 'Gabapentin Capsules, USP, 100 mg, 100 capsules (10x10)' in blister pack cartons with lot number M05205 and expiration date 10/2026.
The recall does not specify a remedy, so contact Harvard Drug Group for further instructions.
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-0507-2025 — Harvard Drug Group Harvard Drug Group Hello, I own a Harvard Drug Group that is covered by recall D-0507-2025 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.
