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Boscogen Inc

FEI 1000519929 · 8 Chrysler, Irvine, California, 92618, 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
2026-04-21
6 months ago

FDA record

  1. 2026-04-21
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  2. 2019-09-30
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  3. 2016-05-26
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Foodborne Biological Hazards
    FDA source
  4. 2007-06-11
    RecallRecall F-465-7 · Class 1 · Testing performed recently at NBTY, Inc. (the manufacturer) shows that the recalled capsules have the potential to be contaminated with Salmonella. Although multiple lot numbers may have been involved in the recall by NBTY, only NBTY lot number 64951 was purchased, repacked and distributed by Boscogen, Inc as Lynae Shark Cartilage 750mg, Lot Number FJ04101F, Expiration Date 12/2008.
    Lynae Shark Cartilage 750mg Capsules, Product Number FS1001, Lot Number FJ04101F, Expiration Date 12/2008, UPC Number 85714 00282 2, 100 capsules per bottle
    Source: FDA Enforcement Reports