FDAOctober 18, 2019device

Energy FX: a) original Aluminum (100-3A) b) sleek (adult and kid & pet) (100-3B)

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

FDA determined that marketing claims surrounding product rendered product a medical device which was adulterated and misbranded.

What to do

FDA enforcement status: Completed

Brands named

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Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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