BTREX PLUS Dietary Supplement 2 Caplets
Reason CGMP Deviations: Presence of damaged tablets
Recalled by Lopez Gonzalez Santana Corporation · Rio Piedras, PR, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
CGMP Deviations: Presence of damaged tablets
These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.
BTREX PLUS, Dietary Supplement 100 Caplets
Quantity: 662 bottles.
Food: Dietary supplements
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot # 33491, Exp. 12/22
Puerto Rico
FDA's distribution note: Domestic distribution only-PR
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
FDA files each product of one recall action separately; these share the same FDA event.
Reason CGMP Deviations: Presence of damaged tablets
Reason CGMP Deviations: Presence of damaged tablets
Reason CGMP Deviations: Presence of damaged tablets
Reason cGMP Deviation: Presence of damaged tablets
Reason Label does not declare walnuts in English
Reason Label does not declare walnuts in English
Reason Label does not declare walnuts in English
Reason Possible Salmonella in Moringa Leaf Powder product.