Class II · Moderate risk Terminated Other Aug 2, 2017
Reason The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to possible product contamination with…
Class II · Moderate risk Terminated Other Aug 2, 2017
Reason The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to possible product contamination with…
Class II · Moderate risk Terminated Other Aug 2, 2017
Reason The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to possible product contamination with…
Reason Undeclared allergens: soy (lecithin)
Reason Undeclared allergens: soy (lecithin)
Reason Undeclared allergens: soy (lecithin)
Reason Undeclared allergens: soy (lecithin)
Reason Undeclared allergens: soy (lecithin)
Reason Undeclared allergens: milk (Colostrum)
Reason Undeclared allergens: milk (Whey)
Reason Undeclared allergens: milk (Colostrum, Dried Yogurt, Whey).
Class II · Moderate risk Terminated Processing Jul 21, 2017
Reason Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
Class II · Moderate risk Terminated Processing Jul 21, 2017
Reason Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
Class II · Moderate risk Terminated Labeling Jul 21, 2017
Reason Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not declare milk.
Reason Grandmas Herbs Cholesterol has undeclared soy lecithin.
Class I · High risk Terminated Salmonella Jun 11, 2017
Reason Product may be contaminated with Salmonella.
Reason Product contains undeclared milk.
Class I · High risk Terminated Other May 23, 2017
Reason MusclMasster, LLC is recalling all bottles of Al-Er-G Capsules because they contain the presence of Ephedra Herb, an FDA banned ingredient.
Class II · Moderate risk Terminated Hidden drug May 22, 2017
Reason Product contains DMAA and Methylsynephrine.
Class II · Moderate risk Terminated Labeling May 12, 2017
Reason During production of St. John's Wort, Lot 160876, a number of bottles were mistakenly labeled as Calcium D-Glucarate Plus
Class II · Moderate risk Terminated E. coli May 8, 2017
Reason 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Class II · Moderate risk Terminated E. coli May 8, 2017
Reason 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Class II · Moderate risk Terminated E. coli May 8, 2017
Reason 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Class II · Moderate risk Terminated E. coli May 8, 2017
Reason 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Class II · Moderate risk Terminated E. coli May 8, 2017
Reason 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)