Hepatodoron¿ tablets
Reason Dietary supplement may contain metal
Dietary supplements in capsule, tablet and powder form - including products found to contain hidden prescription drugs.
Reason Dietary supplement may contain metal
Reason Colostrum is declared but label does not declare milk.
Reason Bloated Protein Bottle
Reason Bloated Protein Bottle
Reason Bloated Protein Bottle
Reason Product labeled and intended to mitigate, prevent, or treat COVID-19
Reason Raw material tested positive for Cronobacter sakazakii.
Reason High bacterial growth within products
Reason High bacterial growth within products
Reason High bacterial growth within products
Reason The product label claim for copper is 0.5mg, but third-party lab results revealed product contains higher levels of copper.
Reason Physical appearance of bottle of G-Pre Protein was atypical. Once opened, unusual odor was noticed and atypical bubbles were present.
Reason Product's ingredients names such as Oregon Grape, Cayenne Root, and Ginger Fruit and their quantities were not listed correctly in the Supplement Facts panel.
Reason The firm was notified by a customer that the bottle contains green and white capsules instead of the usual white round tablets. They contacted their manufacturer to investigate the issue and the manufacture stated that…
Reason Product spoiling over time; spoilage visible beneath lid/closure upon opening.
Reason The microbial test result is found to be out of specification due to high yeast and mold counts.
Reason Product was labeled as "gluten free" and it may contain gluten.
Reason Product failed micro testing. Firm sent product for destruction, but was redirected for sale through online store.
Reason Potential exposure to rodents and rodent activity in the distribution center.
Reason Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
Reason Undeclared fish allergen
Reason Product bottle has potential to become pressurized over time. When consumer opens a bottle, the cap, capsules, and product powder could be forcefully expelled, and customers may sustain injuries to their hands and eyes.
Reason During an FDA investigation the firm was notified that the product contains undeclared milk.
Reason During an FDA investigation the firm was notified that the product contains undeclared shellfish.
Reason During an FDA investigation the firm was notified that the product contains undeclared milk.