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SensoryEffects, Inc.

FEI 1924499 · 13723 Riverport Dr, Maryland Heights, Missouri, 63043, 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
2026-06-10
4 months ago

FDA record

  1. 2026-06-10
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Foodborne Biological Hazards
    FDA source
  2. 2019-08-29
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Foodborne Biological Hazards
    FDA source
  3. 2016-05-26
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Foodborne Biological Hazards
    FDA source
  4. 2014-04-07
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Foodborne Biological Hazards
    FDA source
  5. 2013-06-18
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Foodborne Biological Hazards
    FDA source
  6. 2012-03-22
    RecallRecall F-1047-2012 · Class 2 · Products contain undeclared fish gelatin
    SensoryEffects Flavor Systems Orange-Peach-Mango Fruit Bar Base, packaged in 50-lb. pails and 495-lb. drums. The firm name on the label is SensoryEffects Flavor Systems, Bridgeton, MO.
    Source: FDA Enforcement Reports
  7. 2012-03-22
    RecallRecall F-1048-2012 · Class 2 · Products contain undeclared fish gelatin
    SensoryEffects Flavor Systems Carrot Cake Flavor Base, packaged in 50-lb. pails. The firm name on the label is SensoryEffects Flavor Systems, Bridgeton, MO.
    Source: FDA Enforcement Reports
  8. 2011-06-29
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Foodborne Biological Hazards
    FDA source
  9. 2011-06-29
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  10. 2010-04-21
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Foodborne Biological Hazards
    FDA source
  11. 2009-01-19
    RecallRecall F-376-9 · Class 1 · The product was manufactured using peanut butter recalled by Peanut Corporation of America because it has the potential to be contaminated with Salmonella
    Peanut Butter Base packaged in 450-lb. containers, for use in further manufacture
    Source: FDA Enforcement Reports
  12. 2009-01-12
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Foodborne Biological Hazards
    FDA source
  13. 2008-05-16
    RecallRecall F-545-8 · Class 3 · Pear concentrate used in the manufacture of the product contained elevated levels of inorganic arsenic
    Natural Caramelized Pear Flavor Base WONF packaged in 5-gal. pails, net wt. 50 lbs.
    Source: FDA Enforcement Reports