Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Gabapentin Tablets USP Recalled by InvaGen Pharmaceuticals, Inc. Due to Failed Impurities/Degradation Specifications; failure of Impurity A test...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact InvaGen Pharmaceuticals, Inc. directly.
Affected Products
Gabapentin Tablets USP, 600 mg, Rx Only, 500-count bottle, Manufactured for: Exelan Pharmaceuticals, Inc., Lawrenceville, GA 30046, Manufactured by: InvaGen Pharmaceuticals, Inc., Hauppauge, NY 11788, NDC 76282-405-05.
Quantity: 2,202 bottles
Why Was This Recalled?
Failed Impurities/Degradation Specifications; failure of Impurity A test at the 12-month long-term stability testing.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About InvaGen Pharmaceuticals, Inc.
InvaGen Pharmaceuticals, Inc. has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report