Neolife International LLC
FEI 2912990 · 2125 American Ave, Hayward, California, 94545, United States
Per FDA, as of 2026-10-31 · Sources: FDA Data Dashboard, Import Alerts, Enforcement Reports
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Import alerts
0
Import refusals (5 years)
0
Warning letters
0
Last FDA action
2026-09-16
46 days ago
FDA record
- 2026-09-16InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)Project area: Food Composition, Standards, Labeling and EconFDA source
- 2026-09-16InspectionFDA inspection · Classification: No Action Indicated (NAI)Project area: Foodborne Biological HazardsFDA source
- 2020-01-03InspectionFDA inspection · Classification: No Action Indicated (NAI)Project area: Foodborne Biological HazardsFDA source
- 2020-01-03InspectionFDA inspection · Classification: No Action Indicated (NAI)Project area: Food Composition, Standards, Labeling and EconFDA source
- 2017-05-30InspectionFDA inspection · Classification: No Action Indicated (NAI)Project area: Food Composition, Standards, Labeling and EconFDA source
- 2016-06-23RecallRecall F-2154-2016 · Class 1 · Product was manufactured with Sunflower Kernels provided by SunOpta, which are under recall for possible contamination with Listeria Monocytogenes.NeolifeBar: Fruit & Nuts; 10 g Protein; 5 g Fiber. 320 mg Omega-3s. Net Wt. 1.6 oz. (45 g). Product is sold as a package of 15 bars: Distributed by GNLD International, LLC, Fremont, CA. Not sold in retail storesSource: FDA Enforcement Reports
- 2014-06-02InspectionFDA inspection · Classification: No Action Indicated (NAI)Project area: Foodborne Biological HazardsFDA source
- 2014-06-02InspectionFDA inspection · Classification: No Action Indicated (NAI)Project area: Food Composition, Standards, Labeling and EconFDA source
- 2012-04-20InspectionFDA inspection · Classification: No Action Indicated (NAI)Project area: Foodborne Biological HazardsFDA source
- 2012-04-20InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)Project area: Food Composition, Standards, Labeling and EconFDA source