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Bethel Nutritional Consulting Recalls
5 recalls on record · September 4, 2013 to July 15, 2015 · Drugs
Recalls by year
13
15
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 15, 2015DrugsFDA
Bethel Nutritional Consulting, Inc recalls SLIM-K, 30 Capsules, barcode 160126417509, Distributed by: Bethel Inc.
Hazard: Marketed Without An Approved NDA/ANDA: Product was found to contain sibutramine, desmethylsibutramine and phenolphthalein based on FDA sampling and analysis.
April 1, 2015DrugsFDA
Bethel Nutritional Consulting, Inc recalls B-Lipo, 30 Capsules, Manufactured by KM DALI, Kunming, China for Bethel Nutritional Consulting, Inc.599 West 190th Stree
Hazard: Marketed without an Approved NDA/ANDA; found to contain Lorcaserin, a controlled substance used for weight loss
December 25, 2013DrugsFDA
Bethel Nutritional Consulting, Inc recalls Bethel Advance (bitter orange, mulberry leaf, cassia seed extract, jobstear seed, spirulina, starch, kola nut) capsules,
Hazard: Marketed Without An Approved NDA/ANDA: FDA analyses detected the presence of phenolphthalein, N-di-Desmethylsibutramine, and trace amounts of sibutramine and N-Desmethylsibutramine. Sibutramine and phenolphthalein were previously available drug products but were removed from the U.S. market making these products unapproved new drugs.
December 25, 2013DrugsFDA
Bethel Nutritional Consulting, Inc recalls Quick Thin (citrus aurantium extract, sweet potato fiber, cyamopsis gum powder, alfalfa, mulberry leaf, guarana, spiruli
Hazard: Marketed Without An Approved NDA/ANDA: FDA analysis detected the presence of sibutramine, N-Desmethylsibutramine and phenolphthalein. Sibutramine and phenolphthalein were previously available drug products but were removed from the U.S. market making these products unapproved new drugs.
September 4, 2013DrugsFDA
Bethel Nutritional Consulting, Inc recalls Bethel 30 capsules, packaged in 30 count bottles, Distributed by BETHEL INC. New York, New York
Hazard: Marketed Without An Approved NDA/ANDA: FDA analysis found this product contained undeclared sibutramine and phenolphthalein, two active ingredients that were once marketed in the U.S. but removed due to safety reasons, making this product an unapproved new drug.