Zydot Ultimate Blend Detox Drink Natural Tropical Ice Flavor 32 fl. oz. (946 ml) and 16 fl. oz. (473 ml) packaged in clear plastic bottles
Zydot Unlimited
Undeclared yellow # 5
95,075 total recalls in our database
Zydot Unlimited
Undeclared yellow # 5
The Harvard Drug Group
Microbial contamination of Non-sterile Products; presence of yeast and potential B. cepacia contamination
Labeling: Label Mixup; potentially mislabeled
Microbial contamination of Non-sterile Products; presence of yeast and potential B. cepacia contamination
Microbial contamination of Non-sterile Products; presence of yeast and potential B. cepacia contamination
Failed Impurities/Degradation Specifications:Out of specification results for individual unknown impurities at 30th month Room Temperature Retained Sample stabilities test .
Microbial contamination of Non-sterile Products; presence of yeast and potential B. cepacia contamination
Microbial contamination of Non-sterile Products; presence of yeast and potential B. cepacia contamination
Labeling: Labeled Error on Declared Strength; report of a 1000 ct bottle labeled as Phenobarbital 15 mg tablets actually contained 30 mg tablets
Labeling: Label Mixup; potentially mislabeled
Labeling: Label Mixup; potentially mislabeled
Labeling: Label Mixup; potentially mislabeled
Brian P. Richardson
Marketed without an Approved NDA/ANDA; FDA analysis result found product to contain sildenafil, tadalafil and undeclared milk
Labeling: Label Mixup; potentially mislabeled
Shippert Medical Technologies
Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Shippert Medical Technologies
Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.
Shippert Medical Technologies
Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Alcon Research
Some ORA Carts have the potential to return an incorrect IOL power measurement during cataract surgery. This issue appears to have been caused by a software coding error that results in the lens coefficients for an IOL model being downloaded from the Alcon server in an incorrect order.
The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.