Zero Xtreme branded Nutritional Supplement Recall [US]

US/Silver Spring: Zero Xtreme, a Marathon, Florida establishment, recalls certain batch/lots of Zero Xtreme branded Nutritional Supplement Capsules due to suspected presence of Sibutramine, a controlled substance under FDA regulation that was marketed as an appetite suppressant but withdrawn from the US market in 2010 due to suspected increased risks of Cardiovascular Events and Stroke, all serious health and safety hazards.

FDA: http://ht.ly/InAy30mgeRW

Direct link: https://www.fda.gov/Safety/Recalls/ucm623503.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following over-the-counter (“OTC”) drugs are subject to this recall:

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MyNicNaxs Nutritional Supplement Recall [US]

US/Silver Spring: MyNicNaxs, LLC, a Deltona, Florida establishment, has recalled all lots of various Dietary Supplements due to suspected presence of Diclofenac, Phenolphthalein, Sibutramine and/or Sildenafil, all controlled substances and undeclared active pharmaceutical ingredients (“APIs”). The presence of Diclofenac, Phenolphthalein, Sibutramine and/or Sildenafil in the recalled Dietary Supplements renders them unapproved drugs for which safety and efficacy have not been established and, therefore, subject to recall. Due to their ingredients, these Supplements all pose serious health and safety hazards. FDA: http://ht.ly/zYCx30kVBsI

Direct link: https://www.fda.gov/Safety/Recalls/ucm613197.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following over-the-counter (“OTC”) drugs are subject to this recall (in alphabetical order):

Bella branded Diet Capsule Recall [US]

US/Silver Spring: Bella all Natural, a Los Angeles, California establishment, recalls certain batch/lots of Bella branded Diet Capsules due to suspected presence of N-Desmethyl Sibutramine, an active metabolite of Sibutramine, a controlled substance under FDA regulation that was marketed as an appetite suppressant but withdrawn from the US market in 2010 due to suspected increased risks of Cardiovascular Events and Stroke, all serious health and safety hazards. FDA: http://ht.ly/lVq130iG43F

Direct link: https://www.fda.gov/Safety/Recalls/ucm598087.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following over-the-counter (“OTC”) drugs are subject to this recall:

LaBri’s Atomic & Xplode Supplement Recall [US]

US/Silver Spring: EZ Weight Loss TX LLC recalls all current batch/lots of LaBri’s Body Health brand Atomic and Xplode Dietary Supplements due to the suspected presence of Sibutramine, an appetite suppressant that was withdrawn from the US market in October 2010 for safety reasons. Due to the suspected inclusion of Sibutramine, both of the above Supplements are classed by the US Food and Drug Administration as new drugs for which safety and efficacy have not been established and, therefore subject to recall due to serious health and safety hazards. FDA: http://ht.ly/dfZx30dU5ww

Direct link: https://www.fda.gov/Safety/Recalls/ucm568364.htm

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