Recall -- Firm Press Release

FDA posts press releases and other notices of recalls and market
withdrawals from the firms involved as a service to consumers, the
media, and other interested parties. FDA does not endorse either the
product or the company. This listserv covers mainly Class I
(life-threatening) recalls. A complete listing of recalls can be found
in the FDA Enforcement Report at:
http://www.fda.gov/opacom/Enforce.html

MainStar America, LLC Issues Urgent Voluntary Nationwide Recall of Toothpaste

Contact:
Mr. Ernesto H. Botta
(305) 637-1127

FOR IMMEDIATE RELEASE -- Miami, FL -- June 13, 2007 – MainStar
America, LLC, Miami, Florida, is initiating a nationwide recall in
accordance with the U.S. Food and Drug Administration (FDA) of the
toothpaste made in China involving:

    * Lot #20060708 – Item # 160-850 Dr. Cool Toothpaste 120 GR./4 OZ.
      UPC # 6926597170008
    * Lot #20060708 – Item # 160-852 Superdent Toothpaste 120 GR./4 OZ
      UPC # 6926597170015
    * Lot #20060708 – Item # 160-860 Everfresh Smile2 Toothpaste 25 GR./ 1 OZ.
      UPC # 6926597089539

This recall has been initiated because the products may contain the
poisonous chemical diethylene glycol (DEG). DEG is used in antifreeze
and as a solvent, and is a Central Nervous System depressant and
potent kidney and liver toxin.

PLEASE RETURN ALL PRODUCTS IMMEDIATELY TO THE STORES WHICH YOU PURCHASED THEM.

CONSUMERS WHO HAVE THE PRODUCTS SHOULD STOP USING/ RETURN / THROW AWAY.

Retailers immediately examine your inventory and quarantine product
subject to recall. In addition, if you may have further distributed
this product, please identify your customers and notify them at once
of this product recall. Your notification to your customers may be
enhanced by including a copy of this recall notification.

This voluntarily nationwide recall is being made with the knowledge of
the U.S. Food and Drug Administration. No injuries or illnesses have
been reported to date in connection with this problem.

Adverse Reactions or quality problems experience with the use of this
product may be reported to the FDA's MedWatch Adverse Event Reporting
program either online, by regular mail or fax.

Online: www.fda.gov/medwatch/report.htm
Regular Mail: use postage-paid FDA form 3500 available at
www.fda.gov/MedWatch/getforms.htm
Mail to MedWatch 5600 Fishers Lane, Rockville, MD 20852-9787
Fax: 1-800-FDA-0178

FDA's Recalls, Market Withdrawals and Safety Alerts Page:
http://www.fda.gov/opacom/7alerts.html


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Third, it is accepted as being self-evident." ~ Arthur Schopenhauer


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