Food Recall Check

Dietary supplements recalls

Dietary supplements in capsule, tablet and powder form - including products found to contain hidden prescription drugs.

Dietary supplements recalls · page 19

Class II · Moderate risk Terminated Staphylococcus

Muscle Meds (TM) PERFORMANCE TECHNOLOGIES

Reason A raw material initially failed testing Staphylococcus aureus. A retest was conducted with passing results but an out of specification investigation was not properly conducted leaving concern that the finished product…

Armada Nutrition CO, NJ F-2150-2017
Class II · Moderate risk Terminated Undeclared soy

Pharmanex Cholestin Cholesterol Health

Reason Nu Skin announces a voluntary field action for Pharmanex Cholestin due to undeclared allergen; soy.

Nu Skin Enterprises Inc. Nationwide F-1580-2017
Class II · Moderate risk Terminated Undeclared wheat

Pharmanex BioGinkgo Mental Sharpness

Reason Nu Skin announces a voluntary field action for Pharmanex BioGinkgo due to undeclared allergen; wheat.

Nu Skin Enterprises Inc. Nationwide F-1578-2017
Class I · High risk Terminated Other

Xanthium & Siler Combo

Reason Presence of Ephedrae Herba (ma huang), a FDA Banned Ephedra Alkaloid

Kingsway Trading Inc 17 states F-1577-2017
Class III · Low risk Terminated Other

NOW¿ Multi-Food 1 Tablets

Reason Product's supplement fact panel incorrectly states that the product contains 75 mg (milligrams) of Molybdenum, when it actually contains 75 mcg (micrograms).

NOW Foods Nationwide F-1484-2017
Class III · Low risk Terminated Other

Nature's Wonderland Sinus & Lung Care

Reason There was a mix-up with ingredients used. The product is an herbal blend consisting of 7 different herbs. The blend calls for Ginger Root; however, Ginkgo Leaves was accidentally added.

Penn Herb Company, Ltd. F-1528-2017
Class II · Moderate risk Terminated Hidden drug

Xambo, 80 boxes of bulk capsules

Reason West Coast Laboratories is recalling Xambo and Devagrass because there may be presence of 1,3-dimethylamylamine (DMAA).

West Coast Laboratories Inc F-1430-2017
Class II · Moderate risk Terminated Labeling

Source Naturals Dietary Supplement Vitamin D-3

Reason Testing of Vitamin D-3 as a result of a consumer complaint found specific lots to have lower concentrations than product specifications of ingredient labeling.

Threshold Enterprises Ltd Nationwide F-2178-2017
Class II · Moderate risk Terminated Labeling

Cannibal Ferox Amped

Reason Product was analyzed and found to contain 1,3- dimethylbutylamine which was not declared on the label and is a prohibited substance.

Chaos and Pain Nationwide F-0766-2017
Class III · Low risk Terminated Labeling

Safecor Vitamin B-1

Reason Box labeled Thiamine Hydrochloride instead of Thiamine Mononitrate

Safecor Health, LLC Nationwide F-0606-2017
Class II · Moderate risk Terminated Labeling

Cannibal Riot Super Stimulant Pre-Workout Energy Complex

Reason The products are being recalled because they contain 750 mg of Agmatine and 50 mg 1,3 Dimethylbutylamine per serving which is not declared on the label. 1,3 Dimethylbutylamine is not permitted for use in dietary…

Chaos and Pain F-0082-2017
Class II · Moderate risk Terminated Labeling

Cannibal Riot Super Stimulant Pre-Workout Energy Complex

Reason The products are being recalled because they contain 750 mg of Agmatine and 50 mg 1,3 Dimethylbutylamine per serving which is not declared on the label. 1,3 Dimethylbutylamine is not permitted for use in dietary…

Chaos and Pain F-0081-2017
Class II · Moderate risk Terminated Other

CytoDetox Hydrolyzed Clinoptilolite Fragments

Reason Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Pharmatech LLC FL, MI, MS, OH F-0276-2017
Class II · Moderate risk Terminated Other

Renew HC Hydrolyzed Clinoptilolite

Reason Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Pharmatech LLC FL, MI, MS, OH F-0275-2017
Class II · Moderate risk Terminated Other

Pedia D-Vite Drops

Reason Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Pharmatech LLC FL, MI, MS, OH F-0274-2017
Class II · Moderate risk Terminated Other

Pedia Poly-Vite Drops

Reason Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Pharmatech LLC FL, MI, MS, OH F-0273-2017
Class II · Moderate risk Terminated Other

Pedia Tri-Vite Drops

Reason Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Pharmatech LLC FL, MI, MS, OH F-0271-2017