Black Ant, Mojo Risen Supplement Recall Expands [US]


US FlagUS/Silver Spring: 3474 - BlackAntDietary SupplementEugene Oregon expands its existing recall of African Black Ant, Black Ant and Mojo Risen Dietary Supplements to include all lot numbers due to undeclared drug ingredients, a serious health and safety hazard. FDA: http://ht.ly/xtpPs

Direct link: http://www.fda.gov/Safety/Recalls/ucm399144.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following dietary supplements are subject to this recall:

  • African Black Ant; lots affected: all lots; packaging: small boxes inside large box; pack coloring: red, black and silver; quantity per package: 6 capsules per box, 8 boxes per display unit.
  • Black Ant; lots affected: all lots; packaging: small boxes / tins inside large box; pack coloring: green; quantity per package: 4 capsules per small box, 20 boxes display unit. also packaged in 10 tablets and 10 capsules in a metal container.
  • Mojo Risen; lots affected: all lots; packaging: envelopes inside box; pack coloring: red and white; quantity per package: 2 capsules per envelope, 24 envelopes per display box.

According to the FDA, this recall expands an earlier recall to include all lots of the recalled dietary supplements. The company is recalling these products because FDA analysis has revealed undeclared amounts of the active pharmaceutical ingredients sildenafil and tadalafil, both FDA-approved pharmaceutical ingredients used to treat erectile dysfunction. Conclusive testing has not been done to confirm that the recalled products do, in fact, contain sildenafil and/or tadalafil and this recall is being executed as a precautionary measure.

Sildenafil and tadalafil can pose a threat to consumers because they can interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels. Consumers with Diabetes, high blood pressure, high cholesterol, and heart disease often take nitrates. To date, Eugene Oregon, Inc. has not received any reports of adverse events related to this recall.

To see the original recall, search for “Eugene Oregon” or “Recalls Direct RIN: 3474-2014” using the Search Box at the top of this page.

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Recalls Direct RIN: 3589-2014
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Visit the Living Safely site: http://www.LivingSafely.org/
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