TruVision Health Truvy Boost 30-Day Experience Kit recall — FDA F-0948-2023
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Complete FDA and NHTSA recall records dated in May 2023.
These records include useful source details for the selected month.
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Product may exceed FDA guidance levels for leachable lead.
Possible presence of foreign material (metal)
Possible contamination with Listeria monocytogenes
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Undeclared milk
Tarragon Chicken Salad Sandwich label declares Mayonnaise and Bread, but label does NOT declare Egg and Wheat.
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Product packaged into incorrect labeling resulting in undeclared milk protein
Possible contamination with listeria monocytogenes
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Possible contamination with listeria monocytogenes
Possible presence of foreign material (metal)
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Possible contamination with listeria monocytogenes
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Undeclared peanut and soy.
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Undeclared allergen; sesame seeds
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Product may be become pressurized from fermentation and pose a safety risk to consumers who may sustain injuries to their eyes, face, and hands when opening the bottles.
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.