Samurai-X
Marketed Without An Approved NDA/ANDA
18,003 recalls, newest first
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Marketed Without An Approved NDA/ANDA
Defective Delivery System: Firm recalled Guaifenesin liquid and Guaifenesin DM liquid due incorrect dose markings on the dosing cups.
Defective Delivery System: Firm recalled Guaifenesin liquid and Guaifenesin DM liquid due incorrect dose markings on the dosing cups.
Labeling: Incorrect Barcode: Primary bag labeling may be mislabeled with the wrong barcode which scans in as heparin sodium.