Pentrexyl Forte Natural Recalled due to Possible Packaging Confusion with an Antibiotic

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Pharmacists and consumers are informed by the FDA that Pentrexyl Forte Natural is recalled because misleading packaging can cause confusion with an antibiotic leading to delayed treatment.

Background of Pentrexyl Forte Natural

Pentrexyl Forte Natural, by Phoenix Import & Distribution LLC, is a dietary supplement, packaged in a green and white box which contains 30 red and white capsules.

The product was sold in Texas  via retail stores.

FDA Alert on Pentrexyl Forte Natural

The FDA informs that the packaging of Pentrexyl Forte Natural is believed to be misleading, and this may lead to confusion of the product with an antibiotic. Since Pentrexyl Forte Natural is not an antibiotic, its use by patients can delay their treatment for serious illnesses.

Recommendation on Pentrexyl Forte Natural

“Consumers who have purchased the product can return it to the place where it was purchased.”

Contacting the FDA to report cases with Pentrexyl Forte Natural

In case of detection of adverse events or side effects related to the use Pentrexyl Forte Natural, healthcare professionals and patients should report it to the FDA’s MedWatch Safety Information and Adverse Event Reporting program through any of the following ways:

The report can be completed and submitted online at: www.fda.gov/MedWatch/report.htm

The form can be downloaded or requested by calling 1-800-332-1088, then completed and returned on the address indicated on the form

The completed form can be faxed to: 1-800-FDA-0178

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