Company Announcement. For Immediate Release. Contact. Announcement

Similar documents
Detox Transforms Health and Nutrition Issues Voluntary Nationwide Recall of Dietary Supplements Due to the Presence of Undeclared Drug Ingredients

Product NDC Code Lot Number Expiry Dates Distribution Date VALSARTAN TABLETS 40MG 30CT

2 Mylan Valsartan/Combination Class 2 Recall

Contacts Consumers:

FOR IMMEDIATE RELEASE

Magnesium Sulfate in Water for Injection is indicated for the prevention and control of seizures in preeclampsia and eclampsia, respectively.

Hospira Issues A Voluntary Nationwide Recall For 8.4% Sodium Bicarbonate Injection, USP,

BAXTER INITIATES VOLUNTARY NATIONWIDE RECALL OF SELECT LOTS OF IV SOLUTIONS DUE TO THE POTENTIAL FOR LEAKING CONTAINERS AND PARTICULATE MATTER

TreeHouse Foods Amends Best By Dates in Voluntary Product Recall of Macaroni & Cheese Cup Products

POLICY AND PROCEDURE DOCUMENT NAME: Drug Recall Notification Process

Butala Emporium, Inc. Recalls Eleven Ayurvedic Dietary Supplements Because of Elevated Levels of Lead and Mercury

URGENT: DIETARY SUPPLEMENT RECALL

Allergan s Blephamide (sulfacetamide/prednisolone ophthalmic ointment) 10%/0.2%, 3.5Gm tube

URGENT: Important Safety Information

Urgent field safety notice

US FDA/CDRH: Public Health Notification: Serious Complications Associated with Transvaginal Place... FDA Home Page CDRH Home Page Search A-Z Index

Supporting our provider partners through communication and collaboration. Formulary Updates

If you have any questions, please contact Jerry Webb at ext or

Urgent field safety notice

Recall -- Firm Press Release

URGENT: Important Safety Information

URGENT: VOLUNTARY DRUG RECALL 07/05/2016

Effexor XR 150mg and one lot of Greenstone Venlafaxine 150mg extended-release capsules

Guidelines for Product Recall or Withdrawal

March 21, Subject: Availability of Blister-Packaged XELODA (capecitabine) Tablets

Suspected Defective Product Report

Iron treatment for people with chronic kidney disease (CKD)

IMPORTANT DRUG WARNING

New York State Department of Health. Notice of Voluntary Recall of Influenza A (H1N1) 2009 Monovalent Vaccine

Guidelines for the Recall or Withdrawal of a Medical Product

ALLERGIES ARE OUT THERE.

2. Receive the Guidelines for the Allergist letter which is to be given to the prescribing allergist physician.

Maternity Services Intravenous iron therapy Information for women

ORDER of the Minister of Health No. 269/2017 of 14 March 2017 on mandatory provision of medicinal product adequate and continuous supplies

INTRAVENOUS IRON THERAPY

SPCA Event Sponsor Information

September page 1 / 15

INFORMATION SHEET FOR THE DEPARTMENT OF PAIN AND PALLIATIVE CARE

PRODUCT RECALL NOTICE URGENT

AFDO Conference June 9, Mercedes Mota, Director Medical Device, Surgical Care Johnson & Johnson Quality & Compliance Worldwide

IMPORTANT DRUG INFORMATION

Please see the attached for specific SKUs, location of lot code data and expiration dates of impacted products.

American Emu Association. Certified Emu Oil Program

GENERAL INFORMATION AND INSTRUCTIONS

URGENT FIELD SAFETY NOTICE

Enforcement Report - Week of November 1, 2017

Douglas V. Faller, Ph.D., M.D., Susan P. Perrine M.D.

ZINBRYTA REMS (Risk Evaluation and Mitigation Strategy) Program Patient Guide

June 9, PET FOOD INSTITUTE 2025 M Street, NW, Suite 800 Washington, DC M Street NW Suite 800 Washington, DC Page 1 of 6

Recall Guidelines. for Chinese Medicine Products

NAMI California Peer-to-Peer Mentor Training Application

4/26/2013. Libia Lugo Drug Specialist San Juan District Office Investigations Branch

Your pet s diabetes is manageable

Enjoy the purrfect value in test strips for your pets at the lowest price for use with AlphaTRAK and AlphaTRAK 2 Meters

Health Authority Abu Dhabi. Document Title: Policy for Recall of Drugs and Healthcare Products Document Ref. Number:

February 27, Human Use. Dear Sir or Madam: new data and. responded to. United States. the United products.

The pages that follow contain information critical to protecting the health of your patients and the citizens of Colorado.

Thank you for downloading this patient assistance document from NeedyMeds. We hope this program will help you get the medicine you need.

INFORMATION AND CONSENT FORM For Adults Aged 18 and Older Additional Facility Sites

AMERICAN CANCER SOCIETY FUNDRAISING APP FAQS

Varicose vein treatment radiofrequency ablation (ClosureFast)

Class I Drugs Event Event ID: Product Type: Status: Date Terminated: Recall Initiation Date: Voluntary / Mandated: Center Classification Date:

Azelastine Nasal Spray 1 mg / 1 ml

HeartMate 3 Left Ventricular Assist System Catalog #106524US LVAS KIT, HM3

Please describe, in detail, when the symptoms began:

Exhibitor Registration Application NCCTA Winter Meeting and Trade Show March 1-2, 2018 Meadowbrook Inn, Blowing Rock, NC

ALECENSA (alectinib) oral capsule

THE VETERINARY GUIDE TO TEAR STAINING. By John Burns BVMS MRCVS. Natural nutrition for a long healthy life

Dispensing and administration of emergency opioid antagonist without a

JYNARQUE REMS (RISK EVALUATION AND MITIGATION STRATEGY) PATIENT GUIDE

Pediatric Intake Paperwork. Personal History

TRANSFUSION ASSOCIATED DISEASE, RECALL, OR COMPLICATION INVESTIGATION POLICY I. FATALITIES AND COMPLICATIONS ASSOCIATED WITH TRANSFUSION:

Urgent Field Corrective Action

Center for Family Health Policy

Product Recalls. Protecting Public Health. Presented by William Stewart & Thomas DiBruno

URGENT FIELD SAFETY NOTICE/ DEVICE RECALL

Patient Name: Date: Address: Primary Care Physician: Online Website On TV In print On the radio

2015 NLN Marketing Options

Authorization and appeals kit: Psoriatic arthritis

2016 Travelers Prescription Drug Plan Blue Cross Blue Shield Plan and United Healthcare Choice Plus Plan

PATIENT QUESTIONNAIRE

MEDICATION MANAGEMENT AGREEMENT Pain Management Program Participation Agreement and Consent

Authorization and appeals kit: Moderate to severe plaque psoriasis coexisting with psoriatic arthritis

February is National Dental Health Awareness Month!

Valium for stomach pain

Indication. Important Safety Information

Product Correction Urgent Immediate Action Required

L A W O F F I C E S HYMAN, PHELPS & MCNAMARA, P.C.

Unofficial translation /Ministry of Social Affairs and Health. No. 548/2008. Government Decree on Narcotics Control

Date of Birth: Phone: ( ) Gender: M F. City: State: Zip:

Treatment Journal. Therapy Tracker TREATMENT JOURNAL

Gabapentin 10 mg for dogs side effects

Medications for Alzheimer s disease: are they right for you?

STATE OF NEW JERSEY Division of Gaming Enforcement CASINO HOTEL ALCOHOLIC BEVERAGE MERCHANDISING PERMIT APPLICATION

Peripheral neuropathy

In Your Face: Makeup Contaminated With Asbestos

clonazepam and xanax and mirtazapine, mirtazapine remeron werking everything about mirtazapine, cheap mirtazapine mirtazapine metoprolol.

Experience the ultimate test strip for use with OneTouch Ultra, Ultra 2, and UltraMini meters

INTRODUCTION TO DRUG LAW AND REGULATION: REGULATION OF DRUG MANUFACTURING

FREQUENTLY ASKED QUESTIONS FOR MARIJUANA ESTABLISHMENTS

Transcription:

Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. For Immediate Release October 3, 2018 Contact Consumers remedies@silverstarbrands.com 1-888- 736-6389 Announcement Silver Star Brands, Inc., is initiating a voluntary recall of six products for humans (including four and two Healthful Naturals ) and two PetAlive products for pets for a total of eight products with lot numbers, see table below, to the consumer level. The products have been tested and found to contain microbial contamination. Administration of or use of drug products with microbial contamination could potentially result in increased infections that may require medical intervention and could result in infections that could be life threatening to certain individuals and animals. To date, Silver Star Brands, Inc. has not received any reports of adverse events related to this recall. These products can be identified by the main label on the bottle and the lot number that is printed on the label. Each product recalled is an individual 2 oz. in amber bottle (see table below), manufactured at the King Bio, Inc. facility in Asheville, NC. Product was distributed nationwide via wholesale, retail and online sales., PetAlive and Healthful Naturals package images for products affected are attached (below).

HUMAN PRODUCTS PRODUCT INDICATION NDC UPC LOT EXPIRATION DATE VertiFree VaricoGo HypoSlim Temporary relief for dizziness and nausea Relieves discomfort associated with varicose veins Assists with healthy weight management and metabolism 68703-253-02 818837012260 K061417B 6/20 68703-105-59 818837010419 K111717A 11/20 68703-275-02 818837013724 K051818A 05/21 EyeClear Pro oral spray Relieves symptoms of mineral buildup and eye irritation 68703-151-59 818837011652 K022317A, K022317B 02/20 Healthful Naturals DizziFree Healthful Naturals Leg Cramp Support Temporarily relieves dizziness and nausea Temporary relief from cramps and spasms while resting 68703-204-02 840853166535 K022616D N/A 68703-206-02 840853166559 K022216C N/A PET PRODUCTS PRODUCT INDICATION NDC UPC LOT EXPIRATION DATE PetAlive Plump-Up Pet PetAlive Allergy Itch Ease oral spray Improves appetite in underweight dogs and cats Relieves skin itch 68703-290-02 818837013908 K011617E 01/20 68703-135-59 818837011102 K111617B 11/20

Silver Star Brands, Inc. is notifying its distributors and customers by letter and is arranging for return and replacement (or refund) of the recalled products. Consumers/distributors/retailers that have this product which is being recalled should discontinue use/ distribution and contact Silver Star Brands, Inc. at remedies@silverstarbrands.com to make arrangements to return th product. These products were distributed to retailers (doctor offices, pharmacies, health food stores) and consumers (direct sales and website). Consumers with questions regarding this recall can contact Silver Star Brands, Inc. at 1-888- 736-6389 Monday Friday 8:00 am 5:00 pm CST or email reme-dies@silverstarbrands.com. Consumers should contact their physician or healthcare provider if they believe they have experienced any problems that may be related to using this product. Adverse reactions or quality problems associated with the use of this product may be reported to FDA's MedWatch Adverse Event Reporting program either by phone, on line, by regular mail or by fax. Complete and submit the report Online: www.fda.gov/medwatch/report.htm (http://www.fda.gov/medwatch/report.htm) Regular Mail or Fax: Download form www.fda.gov/medwatch/getforms.htm (http://www.fda.gov/medwatch/getforms.htm) or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178. The Center for Veterinary Medicine recommends calling the drug company to report adverse drug experiences or product defects for FDA-approved animal products. The drug company responsible for the approved product is required to submit these reports to FDA. Call1-888-736-6389. If you prefer to report directly to the FDA, you can submit Form FDA 1932a by following the link to the form found at https://www.fda.gov/animalveterinary/safetyhealth/reportaproblem/ucm055305.htm and following the instructions for emailing the completed form to FDA. If you have a question about ADE reporting or need a paper copy of the form, contact CVM by email at AskCVM@fda.hhs.gov or by phone at 1-888-FDA-VETS (1-888-332-8387). ###

5 of 6 10/4/2018, 7:20 PM