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NBTY, Inc.

FEI 2413835 · 110 Orville Dr, Bohemia, NY, United States

1 import refusal on record (5 years)

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)
1
Warning letters
0
Last FDA action
2026-08-03
3 months ago

FDA record

  1. 2026-08-03
    Import refusalShipment refused · FDA charge codes: 260,482 · Product: MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN)
    Shipment line 9DH-0081162-5/20001/1 · Product code 54ACH90
    FDA source
  2. 2024-03-18
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  3. 2021-07-09
    RecallRecall F-0789-2021 · Class 3 · Vitamin D dietary supplement may contain Coq10
    Kroger brand, Vitamin D3 125 mcg softgels, 100 count, Green HDPE packaging
    Source: FDA Enforcement Reports
  4. 2019-07-18
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  5. 2016-11-03
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  6. 2016-11-03
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  7. 2016-09-23
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  8. 2016-09-23
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Foodborne Biological Hazards
    FDA source
  9. 2015-10-28
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  10. 2014-11-14
    RecallRecall F-0710-2015 · Class 1 · NBTY has recalled ABC Dophlius Powder due to the presense of Rhizopus oryzae fungi.
    SOLGAR ENHANCED SERIES ABC DOPHILUS POWDER FOR INFANTS AND CHILDREN, NET WT. 1.75 oz (50 g), UPC 0 33984 00010 0. Carefully Manufactured by: Solgar, Inc., 500 Willow Tree Road Leonia, NJ 07605 U.S.A.
    Source: FDA Enforcement Reports
  11. 2013-12-20
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Foodborne Biological Hazards
    FDA source
  12. 2013-12-20
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  13. 2012-07-02
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  14. 2012-07-02
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Foodborne Biological Hazards
    FDA source
  15. 2012-03-01
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  16. 2012-01-06
    RecallRecall F-0859-2012 · Class 1 · Rexall brand Calcium 1200mg liquid softgels 60-count bottles, lot 387651, actually contain Glucosamine Chondroitin with MSM tablets.
    Rexall liquid filled absorbable Calcium 1200 mg plus 1000 IU Vitamin D3 per serving, 60 Softgels, Dietary Supplement, UPC 301220452113, Prod. No. 45211 --- Manufactured by Rexall Sundown, Inc., 1111 SW 30th Ave, Deerfield Beach, FL 33442
    Source: FDA Enforcement Reports
  17. 2011-08-31
    RecallRecall F-1776-2011 · Class 2 · Undeclared wheat discovered during internal review.
    Good 'N Natural label Brewer's Yeast Powder Dietary Supplement, Net Wt. 1 lb. (16 oz.)(453 or 454 g), Item # 2270, UPC 0 74312 42270 6, Carefully Manufactured by Good 'N Natural Manufacturing Corp. Holbrook, NY 11741
    Source: FDA Enforcement Reports
  18. 2011-07-21
    RecallRecall F-1636-2011 · Class 1 · Undeclared fish gelatin from Vitamin E raw material.
    sunmark brand multiple vitamin Women's, DIETARY SUPPLEMENT, MULTIVITAMIN/MULTIMINERAL SUPPLEMENT, 100 TABLETS, UPC 0 10939 41344 4, 49348-967-10, Distributed By: McKesson, One Post Street, San Francisco, CA 94104
    Source: FDA Enforcement Reports
  19. 2011-06-07
    RecallRecall F-1564-2011 · Class 3 · Labeling error; The label incorrectly represents the capsules as containing 2.5 mg of lycopene and 2.5 mg of beta sitosterol per two capsules.
    SPRING VALLEY brand Saw Palmetto 450 mg Herbal Supplement 100 CAPSULES, UPC Code 6 81131 11139 3 -- MANUFACTURED BY: US Nutrition, Inc. Bohemia, NY 11716-2510 (US Nutrition is a division of NBTY, Inc.)
    Source: FDA Enforcement Reports
  20. 2011-06-07
    RecallRecall F-1638-2011 · Class 1 · Undeclared fish gelatin from Vitamin E raw material.
    Daily Multiple Vitamins for Women's 50+ Dietary Supplement, distributed under the following labels, product numbers, and sizes: (a) CVS pharmacy label DAILY MULTIPLE FOR WOMEN 50+, DIETARY SUPPLEMENT, 50 Tablets, Product No. 17850, UPC 0 50…
    Source: FDA Enforcement Reports
  21. 2011-02-08
    RecallRecall F-0484-2011 · Class 2 · Testing performed on a sample showed that it has the potential to be contaminated with Salmonella.
    Super Detox Tea for Dieters is sold under the trademark "Detoxapure". The product is packaged in a green cardboard box containing 30 herbal tea bags, Net Wt. 2.64 oz (75g). One serving size (one tea bag) consists of 2.5g of Detoxapure Pro…
    Source: FDA Enforcement Reports
  22. 2011-01-06
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  23. 2011-01-06
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Pesticides and Chemical Contaminants
    FDA source
  24. 2010-11-04
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  25. 2010-06-03
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  26. 2010-06-03
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Foodborne Biological Hazards
    FDA source
  27. 2008-11-25
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  28. 2007-05-16
    RecallRecall F-462-7 · Class 1 · The product may be contaminated with Salmonella.
    Shark Cartilage Capsules, 740 mg, packaged & distributed under the following private labels (divisions of NBTY): (1) Puritan's Pride brand Shark Cartilage Capsules, Product No. 6580, 100 Capsule Size, UPC 74312 16580 1; (2) Good 'N Natural …
    Source: FDA Enforcement Reports