• About Us
  • Home
Friday, June 9, 2023
No Result
View All Result
NEWSLETTER
WiredNewsEngine
  • Home
  • Press Release
  • Entertainment
  • Health
  • Legal
  • Business
  • Featured
  • Current
  • Home
  • Press Release
  • Entertainment
  • Health
  • Legal
  • Business
  • Featured
  • Current
No Result
View All Result
WiredNewsEngine
No Result
View All Result
Home Legal

FDA expands STEAM dietary supplement recall

by WebMaster
September 28, 2009
in Legal, Press Release
0
0
SHARES
0
VIEWS
Share on FacebookShare on Twitter

The FDA expanded recall to include an additional lot of STEAM, a supplement marketed for erectile dysfunction (ED).

New York product liability attorney alert-Food and Drug Administration (FDA) expands ED dietary supplement product recall with undeclared tadalafil ingredient.

Freeport, NY–Nutracoastal Trading LLC, a Delaware company, has expanded its recall of STEAM, their dietary supplement product. The original recall was announced on July 28th, 2009. The most recent voluntary recall was issued after safety regulators discovered that Lot 90260 contained an undeclared active ingredient, Tadalafil. Tadalafil was omitted from the product label, making STEAM DIETARY SUPPLEMENT an unapproved drug by the U.S. Food and Drug Administration (FDA) www.fda.gov. Tadalafil is found in Viagara, a drug for erectile dysfunction (ED). When taken with nitrates, Tadalafil may cause adverse reactions, such as a drop in blood pressure. Nitrates are often ingested by patients with heart disease, high cholesterol, high blood pressure, or diabetes. Some side effects of the recalled supplement include flushing and headaches. The FDA announced the expansion of the recall to include Lot 90260 on August 21, 2009.

The following item is under federal recall:

– STEAM in white plastic bottles. A bottle contains 5 capsules. The bottle bears the following lot number, expiration date, and UPC code, respectively: 90260, 6 11, and 8 52263 30033 1

The recalled supplement product was sent to retailers across the nation. No illnesses related to the consumption of the product have been reported. The Delaware firm urges consumers to stop taking the supplement. Those who have become ill after taking the supplement should contact their doctor immediately. Illnesses related to the recalled product should be reported online to the FDA’s MedWatch Adverse Event Reporting program. Consumers can also call the FDA, mail the postage-paid FDA form 3500, or fax the form to the FDA. Additional instructions can be found at http://www.fda.gov/Safety/Recalls/ucm179964.htm. Consumers negatively affected by the recalled product may be entitled to compensation for damages.

Staff writer reporting for New York product liability attorney news.

WebMaster

WebMaster

Next Post

Florida SUV accident - Lee County patrol car kills Fort Myers man

Popular News

  • Silencil Reviews – Does It Silence Tinnitus for Real?

    0 shares
    Share 0 Tweet 0
  • Clinitron Bed Management For Flap Patients Is The Standard Of Care

    0 shares
    Share 0 Tweet 0
  • How Substance Abuse Causes Risky Behavior

    0 shares
    Share 0 Tweet 0
  • Organic Green CBD Review: Is OrganicGreen Hemp CBD Oil Safe?

    0 shares
    Share 0 Tweet 0
  • Ceremony CBD Oil Reviews: Trustworthy Hemp CBD Liquid Drops?

    0 shares
    Share 0 Tweet 0

Rehabs Near Me Launches New Rehab Services in the US

February 25, 2021

Ginger-Powered Recoup Beverage: A Founder’s Unlikely Story of Survival and Success

February 13, 2021

What is Unix: The Base of All Operating Systems?

February 2, 2021

Categories

  • Banking
  • Bollywood
  • Brand Partner Content
  • Business
  • Cancer
  • Current
  • Entertainment
  • Featured
  • Finance
  • Health
  • Hollywood
  • Legal
  • Press Release
  • Technology
  • World News
  • Home
  • Press Release
  • Entertainment
  • Health
  • Legal
  • Business
  • Featured
  • Current

No Result
View All Result
  • About Us
  • Home