The Food and Drug Administration used its new powers granted by the Food Safety Modernization Act (FSMA) for just the second time in forcing a company to recall a popular dietary supplement last week. The FDA stated in its letter to USPlabs LLC that its OxyElite Pro dietary supplements have been linked to liver problems, including liver failure. The October death of a woman in Hawaii is blamed on this defective product. Twenty-seven victims have been identified in Hawaii alone, but there are victims in several other states. The FDA also stated that if USPLabs LLC did not recall the adulterated supplements, the FDA would order a halt in distribution, as well as notify distributors and retailers to stop selling the supplements. The products affected by the recall include:
- OxyElite Pro Super Thermo capsules
- OxyElite Pro Ultra-Intense Thermo capsules
- OxyElite Pro Super Thermo Powder