Gabapentin is a medication commonly prescribed for nerve pain. We track every FDA enforcement recall involving Gabapentin (Neurontin) — 17 recalls in our database, including 7 active.
Add Gabapentin to your medicine cabinet and we’ll email you the moment the FDA issues a new recall — before your pharmacy calls. Free forever, no credit card.
The Harvard Drug Group LLC — Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .
Recall D-0031-2026
The Harvard Drug Group LLC — Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .
Recall D-0030-2026
The Harvard Drug Group LLC — Defective container; blister packaging inadequately sealed.
Recall D-0507-2025
The Harvard Drug Group LLC — Defective container; blister packaging inadequately sealed.
Recall D-0508-2025
Glenmark Pharmaceuticals Inc., USA — CGMP Deviations
Recall D-0320-2025
SUN PHARMACEUTICAL INDUSTRIES INC — Cross Contamination
Recall D-0311-2025
SUN PHARMACEUTICAL INDUSTRIES INC — Cross Contamination
Recall D-0312-2025
Granules Pharmaceuticals Inc. — Presence of Foreign Tablets; 3 fused tablets of Metformin ER 500 mg were found in bottle of Gabapentin Tablets
Recall D-0634-2024
Showing 8 of 17. See all Gabapentin recalls.
This page is for information only and isn’t medical advice. Always follow your clinician’s guidance.
The FDA publishes recalls, but most never make the news. The reliable way is an automated alert: sign up free and we’ll email you when a Gabapentin recall is issued.
Most prescriptions filled in the US are generics, so most recalls involve generic products. A recall doesn’t mean the drug itself is unsafe — it usually affects specific lots or manufacturers.
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