Northstar Rx LLC has recalled specific bottles of Gabapentin Capsules, USP 300 mg because consumers complained of receiving empty capsules. The recall affects 24,816 bottles distributed nationwide. This issue relates to failed tablet and capsule specifications rather than a chemical defect in the drug itself. Read more at govinfonow.com/recall/45649-aurobindo-pharma-usa-inc-recalls-gabapentin-capsules-usp-300-mg.
“Northstar Rx Gabapentin Recall: Empty Capsule Complaints.” GovInfoNow, updated October 12, 2026. https://govinfonow.com/recall/45649-aurobindo-pharma-usa-inc-recalls-gabapentin-capsules-usp-300-mg. Based on FDA recall #D-0330-2015 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0330-2015%22&limit=1).
Aurobindo Pharma USA Inc, on behalf of Northstar Rx LLC, recalled Gabapentin Capsules USP 300 mg due to failed specifications involving empty capsules, according to the FDA. The Food and Drug Administration announced the recall on Oct. 17, 2014.
The recall addresses complaints of empty capsules received by consumers. The product failed tablet and capsule specifications.
Context
GovInfoNow's records show Aurobindo Pharma USA Inc has 32 other recalls on record since April 9, 2013. Other recent recalls include a July 23, 2026 recall of Dicyclomine Capsules due to empty capsules and a May 22, 2025 recall of Acetaminophen Tablets for brown tablet discoloration risk. Northstar Rx also issued a Sept. 25, 2026 recall for Tretinoin Cream due to impurities.
How to tell if you have this one
Look for 100-count bottles of Gabapentin Capsules, USP 300 mg manufactured by Aurobindo Pharma Limited for Northstar Rx LLC. Check the label for NDC 16714-662-01, UPC 3 16714-662-01 5, and Lot # GESB14011-A with an expiration date of 12/15.
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.
Official source: FDA Recall #D-0330-2015 (October 17, 2014) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0330-2015 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 12, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
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