💊 Drugs • 12,141 recalls
The One Minute Miracle
Marketed Without An Approved NDA/ANDA: Miracle Diet 30 was found to contain undeclared phenolphthalein, a drug product once contained in over-the-counter laxatives but was taken off the U.S. market due to safety concerns, making this product an unapproved drug.
Labeling: Wrong Bar Code
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Pacific Healthcare, Inc
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Pacific Healthcare, Inc
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility
Pacific Healthcare, Inc
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility
Pacific Healthcare, Inc
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Pacific Healthcare, Inc
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility
The One Minute Miracle
Marketed Without An Approved NDA/ANDA: Miracle Rock 48 was found to contain undeclared thiosildenafil, an analogue of an FDA approved drug for male erectile dysfunchtion making this product an unapproved drug.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Pacific Healthcare, Inc
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility