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...]

      Meijer Issues Recall on Frederik’s Dark Chocolate Almonds Due to Presence of Undeclared Cashews

      Summary Company Announcement Date: June 13, 2025 FDA Publish Date: June … [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 / Drug Recalls / ION Labs Inc. Recalls Influend Cough and Cold Products, in Alabama

ION Labs Inc. Recalls Influend Cough and Cold Products, in Alabama

April 16, 2009 By The FDA Leave a Comment

CONTACT: 877-990-4466

FOR IMMEDIATE RELEASE — CLEARWATER, FL. – APRIL 13, 2009 — ION LABS INC. OF CLEARWATER, FL. IS VOLUNTARILY RECALLING ALL OF THE INFLUEND COUGH AND COLD PRODUCTS SOLD ON OR AFTER MAY 30, 2008. ION LABS INC. IS RECALLING THE LISTED PRODUCTS DUE TO THE PRODUCTS NOT TESTED IN CONFORMANCE WITH THE SPECIFICATIONS OF THE LAB, THEREFORE THE PRODUCTS MAY HAVE A POSSIBILITY TO BE SUPER POTENT. POSSIBLE COMPLICATIONS MAY INCLUDE TACHYCARDIA, PALPITATIONS, ARRHYTHMIAS, CARDIOVASCULAR COLLAPSE WITH HYPOTENSION, HEADACHES, DIZZINESS, ANXIETY, RESTLESSNESS AND NERVOUSNESS. THE FOLLOWING PRODUCTS WERE DISTRIBUTED AND SOLD DIRECTLY TO CONSUMERS IN THE MADISON/HUNTSVILLE, ALABAMA AREA:

INFLUEND COLD AND COUGH, 24 TABLETS, PRODUCT CODE/ LOT # 800074 INFLUEND SEVERE COLD & FLU, 24 TABLETS, PRODUCT CODE/LOT# 800075 INFLUEND JR. COLD & COUGH, 4 OZ. BOTTLE, PRODUCT CODE/LOT# 800076 INFLUEND JR. SEVERE COLD & FLU, 4 OZ. BOTTLE, PRODUCT CODE/LOT# 800077

WHILE NO ILLNESSES HAVE BEEN REPORTED TO DATE, ION LABS, INC. HAS CEASED DISTRIBUTION OF THESE PRODUCTS UNTIL FURTHER NOTICE. CUSTOMERS WHO HAVE THIS PRODUCT IN THEIR POSSESSION SHOULD STOP USING IT IMMEDIATELY AND CONTACT THEIR PHYSICIAN IF THEY HAVE EXPERIENCED ANY PROBLEMS THAT MAY BE RELATED TO TAKING THIS PRODUCT. PLEASE RETURN THE PRODUCT FOR A FULL REFUND TO THE ADDRESS BELOW. ION LABS, INC. 115TH AVE. N. CLEARWATER, FL. 33760 ANY ADVERSE EVENTS THAT MAY BE RELATED TO THE USE OF THIS PRODUCT SHOULD BE REPORTED TO THE FDA’S MEDWATCH PROGRAM BY PHONE AT 1-800-FDA-1088 OR BY FAX AT 1-800-FDA-0178 OR BY MAIL AT MEDWATCH, HF-2, FDA, 5600 FISHERS LANE, ROCKVILLE, MD 20852-9787, OR ONLINE AT THE MEDWATCH WEBSITE AT WWW.FDA.GOV/MEDWATCH CONSUMERS WHO HAVE QUESTIONS ABOUT THE ABOVE RECALL MAY CONTACT ION LABS CUSTOMER SERVICE AT 1-877-990-4466 AND ASK FOR THE QUALITY DIRECTOR AT EXT. (212). HOURS OF OPERATION ARE M-F FROM 8 A.M. TO 5 P.M. EDT.

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: Drug Recalls, Food Recalls

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

Meijer Issues Recall on Frederik’s Dark Chocolate Almonds Due to Presence of Undeclared Cashews

June 13, 2025 By The FDA

Fuentes Farms, LLC Recalls Product Because of Possible Health Risk

June 13, 2025 By The FDA

Turkana Food Inc. Recall Flora Dried Apricots with Undeclared Sulfites on Product Labeling Because of Possible Health Risk

June 12, 2025 By The FDA

Hero Highlight

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Agro Superior Group Recalls Oliver & Smith Mattresses Due to Risk of Serious Injury or Death from Fire Hazard; Violation of Federal Standard for Mattress Flammability

June 11, 2025 By The CPSC

More than One Million Anker Power Banks Recalled Due to Fire and Burn Hazards; Manufactured by Anker Innovations

June 11, 2025 By The CPSC

Mammut Sports Group Recalls Skywalker Pro Via Ferrata Sets Due to Risk of Serious Injury or Death from Fall Hazard

June 11, 2025 By The CPSC

Endless Pools Recalls Manual Retractable Pool Covers Due to Drowning and Entrapment Hazards; Risk of Serious Injury and Death

June 11, 2025 By The CPSC

TTI Outdoor Power Equipment Recalls RYOBI 40-Volt 24-Inch Cordless Hedge Trimmers Due to Laceration Hazard

June 11, 2025 By The CPSC

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Endless Pools Recalls Manual Retractable Pool Covers Due to Drowning and Entrapment Hazards; Risk of Serious Injury and Death

June 11, 2025 By The CPSC

TTI Outdoor Power Equipment Recalls RYOBI 40-Volt 24-Inch Cordless Hedge Trimmers Due to Laceration Hazard

June 11, 2025 By The CPSC

Medtronic Announces Voluntary Recall of Select Newport™ HT70 and Newport™ HT70 Plus Ventilators and Certain Related Newport™ Service Parts

June 11, 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

  • Meijer Issues Recall on Frederik’s Dark Chocolate Almonds Due to Presence of Undeclared Cashews
  • Fuentes Farms, LLC Recalls Product Because of Possible Health Risk
  • Turkana Food Inc. Recall Flora Dried Apricots with Undeclared Sulfites on Product Labeling Because of Possible Health Risk
  • Vita-Warehouse Corp. Issues Allergy Alert on Undeclared Peanut Allergen in ALDI Welby®, Berkley Jensen®, and VitaGlobe™ Vitamin B12 Gummy Products
  • Bugaboo North America Recalls Giraffe High Chairs Due to Risk of Serious Injury or Death from Fall Hazard
  • Agro Superior Group Recalls Oliver & Smith Mattresses Due to Risk of Serious Injury or Death from Fire Hazard; Violation of Federal Standard for Mattress Flammability
  • More than One Million Anker Power Banks Recalled Due to Fire and Burn Hazards; Manufactured by Anker Innovations
  • Mammut Sports Group Recalls Skywalker Pro Via Ferrata Sets Due to Risk of Serious Injury or Death from Fall Hazard
  • Endless Pools Recalls Manual Retractable Pool Covers Due to Drowning and Entrapment Hazards; Risk of Serious Injury and Death
-- 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