Friday
01May2009
Hydroxycut Recall
Fri, May 1, 2009 | Lisa Barger
This morning, the FDA issued a warning to all users of Hydroxycut products due to the potential for liver damage. The distributor, Iovate, has voluntarily recalled the products from the marketplace.
In a statement issued in the official press release, the FDA has this to say, “Adverse events are rare, but exist.”
Please note that this recall covers all Hydroxycut products—including the “shots”, drink packets and caplets.
In a statement issued in the official press release, the FDA has this to say, “Adverse events are rare, but exist.”
Please note that this recall covers all Hydroxycut products—including the “shots”, drink packets and caplets.
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