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Paddock Laboratories, Inc.

FEI 2127022 · 3940 Quebec Ave N, Minneapolis, Minnesota, 55427, 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
2026-04-08
6 months ago

FDA record

  1. 2026-04-08
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Foodborne Biological Hazards
    FDA source
  2. 2026-04-08
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  3. 2010-06-15
    RecallRecall F-2813-2010 · Class 2 · Presence of Foreign Tablets; bottle of Ferrous Gluconate Tablets, USP 324 mg contained Ferrous Sulfate Tablets, USP, (red) instead of Ferrous Gluconate Tablets, USP (green).
    Ferrous Gluconate Tablets USP, 324 mg, Dietary Supplement, Contains: Each tablet contains 324 mg of ferrous gluconate, equivalent to 38 mg of elemental iron, providing 208% of the US recommended daily intake (RDI) of iron for adults and chi…
    Source: FDA Enforcement Reports