FDA MedWatch - Pentrexyl Forte Natural: Recall - Misleading Packaging

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Title: FDA MedWatch - Pentrexyl Forte Natural: Recall - Misleading Packaging
MedWatch logo MedWatch - The FDA Safety Information and Adverse Event Reporting Program

Pentrexyl Forte Natural: Recall - Misleading Packaging

AUDIENCE: Consumer, Pharmacy

ISSUE: Phoenix Import & Distribution LLC and FDA notified the public of a recall for Pentrexyl Forte Natural because the packaging is believed to be misleading, causing it to be confused with an antibiotic.  Pentrexyl Forte Natural is a Dietary Supplement only and does not contain antibiotics. Use of the product by ill individuals could delay treatment for serious illnesses.

BACKGROUND: The product is packaged in a green and white box, containing 30 red and white capsules. The product was sold through retail stores in Texas.

RECOMMENDATION: Consumers who have purchased the product can return it to the place where it was purchased.

Healthcare professionals and patients are encouraged to report adverse events, side effects, or product quality problems related to the use of these products to the FDA's MedWatch Safety Information and Adverse Event Reporting Program:

 

Read the MedWatch safety alert, including a link to the Press Release, at:

http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm256407.htm

 

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http://survey.foreseeresults.com/survey/display?cid=d509U9xg0gZVxkMRcoMsQg==&sid=link&cpp[date]=05_23_2011_1427&cpp[type]=S


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