US Recall News

United States Recall News Alerts for Recalled Drugs, Food, Products, & Vehicles

MENUMENU
  • Home
  • About
    • Advertise
  • Full Recall News Archive
    • Top Story

      J&J Settles Talc Mesothelioma Settlement

      By Sandra Dalton, Staff Writer On January 6, 2020, Superior Court Judge Stephen Kaus announced that Johnson & Johnsons (J&J) had agreed to … [Read More...]

      Tractor Supply Recalls Traveller Aluminum Loading Ramps Due to Fall Hazard

      The ramps cannot withstand the weight of equipment within the limits that are specified on the ramps and can bend or break while in use, posing a fall … [Read More...]

    • More Safety Articles
    • Federal Preemption of State Product Liability Law
  • Drug Recalls
    • Abilify
    • Benicar
    • Fluoroquinolones
    • Invokana
    • Lipitor
    • Nuplazid
    • Opioids
    • OxyContin
    • Pradaxa
    • Proton Pump Inhibitors (PPIs)
    • Risperdal
    • SSRI
    • Symptoms & Side Effects
    • Taxotere
    • Testosterone
    • Uloric
    • Valsartan
    • Xarelto
    • Zofran
  • Medical Devices
    • 3M Earplug
    • 3T Heater-Cooler System
    • Bair Hugger
    • Bipolar Hip System
    • Essure
    • Hip Replacements
    • Implanon
    • IVC Filters
    • Hernia Mesh
    • Power Morcellators
    • Shoulder Implants
    • Transvaginal Mesh
  • Food Recalls
    • FDA Press Releases
    • USDA Press Releases
  • Auto Recalls
    • Air Bags
    • Ignitions
    • NHTSA Press Releases
    • Off-Road Utility Vehicles
    • Snowmobiles
    • Tires
  • Other Products
    • Asbestos
    • Baby Products
    • Pet Products
    • Roundup
    • Talcum Powder
    • Toy Recalls
You are here: Home / Food Recalls / FDA Press Releases / Iovate Health Sciences U.S.A., Inc. Recalls Hydroxycut Products

Iovate Health Sciences U.S.A., Inc. Recalls Hydroxycut Products

May 5, 2009 By The FDA Leave a Comment

CONTACT: JAMIE MOSS 201-493-1027

IOVATE HEALTH SCIENCES USA, INC. OF BLASDELL, NEW YORK AND ONTARIO, CANADA ANNOUNCED TODAY THAT IT IS VOLUNTARILY RECALLING HYDROXYCUT BRANDED PRODUCTS SOLD IN THE UNITED STATES.

IOVATE INITIATED A VOLUNTARY RECALL WHEN IT BECAME AWARE THAT THE U.S. FOOD AND DRUG ADMINISTRATION’S ASSESSMENT OF 23 REPORTS ABOUT CONSUMERS HAVING EXPERIENCED LIVER-RELATED PROBLEMS, AS WELL AS A SMALL NUMBER OF PUBLISHED CASE REPORTS, WAS DIFFERENT FROM IOVATE’S ANALYSIS. ON MAY 1, 2009, THE FDA ISSUED AN ADVISORY WHICH STATES THAT, “ALTHOUGH THE LIVER DAMAGE APPEARS TO BE RELATIVELY RARE, FDA BELIEVES CONSUMERS SHOULD NOT BE EXPOSED TO UNNECESSARY RISK.” THE NUMBER OF ADVERSE EVENT REPORTS DESCRIBED BY THE FDA IS SMALL RELATIVE TO THE MANY MILLIONS OF PEOPLE WHO HAVE USED HYDROXYCUT PRODUCTS OVER THE 7 YEARS REFERENCED BY THE FDA. IOVATE’S OWN ASSESSMENT OF THE POTENTIAL RISK ASSOCIATED WITH THE USE OF THESE PRODUCTS DIFFERS FROM THAT EXPRESSED BY THE AGENCY. EVERY PRODUCT MARKETED BY IOVATE IS EVALUATED DURING ITS DEVELOPMENT FOR THE SAFETY OF ITS INDIVIDUAL INGREDIENTS. ADDITIONALLY, INDEPENDENT THIRDPARTY EXPERTS FROM THE LEADING INDEPENDENT SCIENTIFIC FIRM SPECIALIZING IN INGREDIENT ASSESSMENT, TOXICOLOGY AND PRODUCT SAFETY FOR THE NUTRITIONAL AND PHARMACEUTICAL INDUSTRY REVIEW THE SAFETY OF IOVATE’S INGREDIENTS AND FORMULAS BEFORE PRODUCTS ARE INTRODUCED IN THE MARKETPLACE. ONLY AFTER THIS EXTERNAL REVIEW IS COMPLETED DOES IOVATE RELEASE A FORMULA.

HOWEVER, OUT OF AN ABUNDANCE OF CAUTION AND BECAUSE CONSUMER SAFETY IS IOVATE’S TOP PRIORITY, IOVATE IS VOLUNTARILY RECALLING THESE HYDROXYCUT-BRANDED PRODUCTS.

THE RECALLED PRODUCTS ARE SOLD IN MULTIPLE-COUNT CAPLET AND CAPSULE BOXES AND BOTTLES. THE FDA ADVISORY STATES THAT, “CONSUMERS WHO HAVE THESE PRODUCTS ARE URGED TO STOP USING THEM.” IOVATE IS WORKING WITH THE FDA AND RETAILERS TO ENSURE THAT THESE PRODUCTS ARE QUICKLY AND EFFECTIVELY REMOVED FROM THE MARKET. FOR PRODUCT REFUNDS, CONSUMERS ARE DIRECTED TO RETURN THEIR PRODUCT DIRECTLY TO THE LOCATION WHERE IT WAS PURCHASED. CONSUMERS WITH QUESTIONS ABOUT THE ADVISORY OR RECALL CAN VISIT WWW.HYDROXYCUTINFORMATION.COM FOR MORE INFORMATION. CONSUMERS CAN ALSO CONTACT THE COMPANY BY CALLING 1-877-468-2835 BETWEEN 9 AM AND 5 PM EASTERN STANDARD TIME.

THE LIST OF PRODUCTS BEING VOLUNTARILY RECALLED BY IOVATE:

HYDROXYCUT RAPID RELEASE REGULAR CAPLETS

631656893649 HYDROXYCUT 140CT CAP US 631656833621 HYDROXYCUT 60 GNC US 631656600988 HYDROXYCUT 300CT CAPLETS US 631656890129 HYDROXYCUT 36CT CAP US "WITH CARDS" 631656282245 HYDROXYCUT 160CT CAP US *DISCONTINUED* 631656873214 HYDROXYCUT 58CT CAP US 631656813418 HYDROXYCUT 70CT CAP US 631656808612 HYDROXYCUT 70CT CAPS US *DISCONTINUED* 631656808117 HYDROXYCUT 100 CAP US *DISCONTINUED* 631656818642 HYDROXYCUT 140CT CAP US *DISCONTINUED* 631656882414 HYDROXYCUT 80CT CAPS US *DISCONTINUED* 631656843262 HYDROXYCUT 210CT CAP US 631656828665 HYDROXYCUT 210 CAP US *DISCONTINUED* 631656600582 HYDROXYCUT 60CT + 1 HYDROXYCUT SACHET WB US 631656600476 HYDROXYCUT 72CT + HYDROXYCUT SACHET WB US 631656600483 HYDROXYCUT 100CT CAPLETS US 631656600506 HYDROXYCUT 150CT CAPLETS US 631656601251 HYDROXYCUT 170 CAPLETS US 631656600452 HYDROXYCUT 30CT CAPLETS US

HYDROXYCUT HARDCORE LIQUID CAPSULES

631656600650 HYDROXYCUT HARDCORE 120CT US 631656600834 HYDROXYCUT HARDCORE 210CT US 631656001778 HYDROXYCUT HARDCORE 30CT US 631656601435 HYDROXYCUT HARDCORE 252CT US 631656601848 HYDROXYCUT HARDCORE 30CT US TRIAL – BODYBUILDING.COM 631656601749 HYDROXYCUT HARDCORE 120CT US NEW 631656601763 HYDROXYCUT HARDCORE 252CT US 631656601756 HYDROXYCUT HARDCORE 210CT US NEW

HYDROXYCUT CAFFEINE-FREE CAPLETS

631656801224 HYDROXYCUT CAFFEINE FREE 140CT CAP US 631656821246 HYDROXYCUT CAFFEINE FREE 330CT CAP US 631656801217 HYDROXYCUT CAFFEINE FREE 100CT CAP US 631656801231 HYDROXYCUT CAFFEINE FREE 58CT CAP US 631656899122 HYDROXYCUT CAFFEINE FREE 36CT CAP US 631656600544 HYDROXYCUT CAFFEINE FREE 60CT US 631656600551 HYDROXYCUT CAFFEINE FREE 72CT US 631656600568 HYDROXYCUT CAFFEINE FREE 100CT US

HYDROXYCUT MAX CAPLETS

631656601466 HYDROXYCUT MAX 120CT BONUS + 1HYD MAX SACHET WB US 631656601633 HYDROXYCUT MAX 210CT BONUS + 1 HYD MAX SACHET WB US

HYDROXYCUT REGULAR DRINK PACKET

631656860191 HYDROXYCUT WEIGHT LOSS DRINK MIX 21PK SACHET – WILD BERRY US 631656860313 HYDROXYCUT WEIGHT LOSS DRINK MIX 21PK SACHET – COUNTRY LEMONADE US

HYDROXYCUT HARDCORE DRINK PACKET (IGNITION STIX)

631656701326 HYDROXYCUT HARDCORE DRINK MIX 2.7G SACHET – BLUE RASPBERRY US 631656701319 HYDROXYCUT HARDCORE DRINK MIX 2.6G SACHET – FRUIT PUNCH US 631656760118 HYDROXYCUT HARDCORE DRINK MIX 40PK X 2G SACHET – FRUIT PUNCH US 631656760125 HYDROXYCUT HARDCORE DRINK MIX 40PK X 2G SACHET – BLUE RASPBERRY US

HYDROXYCUT CAFFEINE-FREE DRINK PACKET

631656760095 HYDROXYCUT CAFFEINE FREE DRINK MIX 21PK X 3.6G SACHET – RASPBERRY ICE US

HYDROXYCUT MAX DRINK PACKET

631656860375 HYDROXYCUT MAX DRINK MIX 40PK X 2.4G SACHET – WILD BERRY US 631656860382 HYDROXYCUT MAX DRINK MIX 40PK X 2.7G SACHET – LEMONADE US

HYDROXYCUT LIQUID SHOT

631656800159 HYDROXYCUT WEIGHT LOSS SINGLE SHOT 2OZ – WILD BERRY US 631656860207 HYDROXYCUT WEIGHT LOSS SHOT 2 X 2OZ PK – WILD BERRY US 631656860498 HYDROXYCUT INSTANT WEIGHT LOSS SHOT 12 X 2OZ – WILD BERRY US

HYDROXYCUT MAX AQUA SHED

631656601855 HYDROXYCUT MAX AQUA SHED 60CT CAPSULES US

HYDROXYCUT HARDCORE RTD

631656860436 HYDROXYCUT HARDCORE 4 X8OZ RTD – GRAPE INFUSION US 631656860399 HYDROXYCUT HARDCORE 4 X 8OZ RTD – TRIPLE WILDBERRY US 631656860665 HYDROXYCUT HARDCORE 12-PACK RTD – GRAPE INFUSION US 631656860467 HYDROXYCUT HARDCORE 3 X 4-PACK RTD – GRAPE INFUSION US 631656860443 HYDROXYCUT HARDCORE 3 X 4-PACK RTD – TRIPLE WILDBERRY US 631656860443 HYDROXYCUT HARDCORE 3 X 4-PACK RTD – TRIPLE WILDBERRY US 631656860568 HYDROXYCUT HARDCORE 12-PACK RTD – TRIPLE WILDBERRY US

HYDROXYCUT 24

631656600933 HYDROXYCUT 24 (96 CAPS/ BLISTER PACK) US

HYDROXYCUT CARB CONTROL

631656800036 HYDROXYCUT CARB CONTROL 58CT CAP US 631656800029 HYDROXYCUT CARB CONTROL 100CT CAP US 631656800012 HYDROXYCUT CARB CONTROL 140CT CAP US

HYDROXYCUT NATURAL

631656600889 HYDROXYCUT NATURAL 100CT US

PLEASE NOTE THAT HYDROXYCUT HOODIA AND HYDROXYCUT CLEANSE PRODUCTS ARE NOT INCLUDED IN THIS RECALL; NOR ARE ANY OTHER IOVATE PRODUCTS.

Share this:

  • Click to share on Facebook (Opens in new window) Facebook
  • Click to share on X (Opens in new window) X
  • Click to share on LinkedIn (Opens in new window) LinkedIn
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

Related

Filed Under: FDA Press Releases

About The FDA

The Food and Drug Administration (FDA) is an agency within the U.S. Department of Health and Human Services. It consists of the Office of the Commissioner and four directorates overseeing the core functions of the agency: Medical Products and Tobacco, Foods and Veterinary Medicine, Global Regulatory Operations and Policy, and Operations.

Leave a ReplyCancel reply

This site uses Akismet to reduce spam. Learn how your comment data is processed.

Facebook
Thomas Roney LLC
Economic Consulting

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Tractor Supply Recalls Traveller Aluminum Loading Ramps Due to Fall Hazard

July 16, 2025 By The CPSC

Deale International Recalls CasaClean Handheld Steamers Due to Risk of Serious Burn Injury; Sold on HSN

July 16, 2025 By The CPSC

iStore Magnetic Wireless Power Banks Recalled Due to Fire and Burn Hazards; Imported by Tomauri

July 16, 2025 By The CPSC

Hero Highlight

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

VIVI E-Bikes Lithium-ion Batteries Sold with VIVI E-Bikes Recalled Due to Fire and Burn Hazards; Risk of Serious Injury or Death; Sold by VIVI

July 16, 2025 By The CPSC

Chetak LLC Group Recalls Product Because of Possible Health Risk

July 16, 2025 By The FDA

Krasniy Oktyabr Inc. USA Issues Alert on Eviscerate Dry Salted Vobla “Aral Silver”

July 15, 2025 By The FDA

BD Issues Update to Voluntary Global Recall of Alaris™ and BD Alaris™ Pump Modules Serviced with Legacy Bezel Kit Assemblies

July 15, 2025 By The FDA

World Market Recalls Emek Spread Pistachio Cacao Cream with Kadayif Due to Salmonella Contamination

July 14, 2025 By The FDA

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

BD Issues Update to Voluntary Global Recall of Alaris™ and BD Alaris™ Pump Modules Serviced with Legacy Bezel Kit Assemblies

July 15, 2025 By The FDA

World Market Recalls Emek Spread Pistachio Cacao Cream with Kadayif Due to Salmonella Contamination

July 14, 2025 By The FDA

YoCrunch® Products Voluntarily Recalled by Danone U.S. Due to Potential Presence of Plastic Pieces in Dome Topper

July 14, 2025 By The FDA

Recall News in Your Inbox

Enter your email address to receive automated recall news updates.

Recent Comments

  • Roger McGowan on ABH NATURE’S PRODUCTS, INC, ABH PHARMA, INC., and STOCKNUTRA.COM, INC. Issues Nationwide Recall of All Lots of Dietary Supplement Products
  • Kathryn Moore on FDA Wants Cancer Warning on Breast Implants
  • BRAD on Huge ATV Recall by Polaris – Sportsman and Scrambler
  • Crystal Anderson on Allergan Voluntarily Recalls BIOCELL® Textured Breast Implants and Tissue Expanders
  • Outsourcing Training on The Modern Marketing of Pain
  • SANDRA Collett on Processed Food Preservative Linked to Autism?
  • Eric Karsh on Health Risks of Roundup Go Well Beyond Cancer

Recent Posts

  • Tractor Supply Recalls Traveller Aluminum Loading Ramps Due to Fall Hazard
  • Deale International Recalls CasaClean Handheld Steamers Due to Risk of Serious Burn Injury; Sold on HSN
  • iStore Magnetic Wireless Power Banks Recalled Due to Fire and Burn Hazards; Imported by Tomauri
  • Bexco Enterprises Recalls Kiwi Electronic Recliner and Swivel Gliders with USB Port Due to Overheating Hazard
  • Primark Recalls DTR Stitch 4-pack Scented Highlighters Due to Risk of Phthalate Exposure; Violates Federal Phthalates Ban; Sold by Primark
  • VIVI E-Bikes Lithium-ion Batteries Sold with VIVI E-Bikes Recalled Due to Fire and Burn Hazards; Risk of Serious Injury or Death; Sold by VIVI
  • Chetak LLC Group Recalls Product Because of Possible Health Risk
  • Krasniy Oktyabr Inc. USA Issues Alert on Eviscerate Dry Salted Vobla “Aral Silver”
  • BD Issues Update to Voluntary Global Recall of Alaris™ and BD Alaris™ Pump Modules Serviced with Legacy Bezel Kit Assemblies
-- See More Recall News

Disclaimer: The information contained in these topics is not intended nor implied to be a substitute for professional medical or legal advice, it is provided for educational purposes only. Always seek the advice of your physician or other qualified healthcare provider about any questions you may have regarding a medical condition. Nothing contained in these topics is intended to be used for medical diagnosis or treatment.


ATTORNEY ADVERTISING. The information provided on this website is not legal advice. No attorney-client relationship is formed by the use of this site. It is not stated or implied that a lawyer is certified as a specialist in any particular field of law. No results are guaranteed, and prior results do not guarantee a similar outcome. This site is informational, only, not dispositive; it is up to you to decide whether a particular lawyer is right for you. Use of this site is subject to your agreement to these.


Copyright © 2025 Altrumedia · Terms of Service · Log in