Harvard Drug Group recalls specific lots of 100mg Gabapentin Capsules (Rx only) due to failed impurities during stability testing. Consumers should contact the manufacturer for details.
Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .
Harvard Drug Group is recalling certain lots of 100mg Gabapentin Capsules (Rx only) because routine stability testing found impurities that didn't meet safety standards. This could pose a risk to consumers using the medication.
The recall is based on stability testing showing impurities that didn't meet safety specifications. While the exact nature of the impurities isn't specified, this could potentially affect the medication's safety and effectiveness.
People who have the specific lots of Gabapentin Capsules listed in the recall notice are affected. Those using prescription gabapentin for conditions like neuropathic pain or seizures are at risk.
Check the blister pack for lot numbers: M04950 (exp 01/2026), M04989/M04990 (exp 02/2026), M05056 (exp 04/2026), M05150 (exp 07/2026), M05290 (exp 11/2026), M05312/M05342 (exp 01/2027), or M05369/M05386 (exp 02/2027).
Look for the lot numbers listed in the recall notice to determine if your product is affected.
The recall is due to failed impurities during routine stability testing, which means the medication may not meet safety specifications.
The official recall notice does not specify a remedy or action for affected products.
Yes, check for lot numbers: M04950 (exp 01/2026), M04989/M04990 (exp 02/2026), M05056 (exp 04/2026), M05150 (exp 07/2026), M05290 (exp 11/2026), M05312/M05342 (exp 01/2027), or M05369/M05386 (exp 02/2027).
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-0030-2026 — Harvard Drug Group Harvard Drug Group Hello, I own a Harvard Drug Group that is covered by recall D-0030-2026 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.
