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Browse drug and medication recalls including prescription drugs, OTC medications, and supplements. Stay informed about pharmaceutical safety alerts.
CGMP Deviations: Repackaging firm recalling due to potential product cross contamination concerns at the manufacturer.
CGMP Deviations: Repackaging firm recalling due to potential product cross contamination concerns at the manufacturer.
Out of specification (OOS) for Spectroscopic Identification test by IR.
CGMP Deviations
CGMP Deviations
CGMP Deviations
This recall involves prescription drugs Nurtec ODT 75 mg orally disintegrating tablets sold in cartons containing one blister card of 8 tablets. The tablets are in a non-child resistant blister card packaged in a carton that includes the name of the product, dosage strength, expiration date. The dosage strength and expiration date are printed or stamped on the blister card. The recall includes the following: Product Description NDC Number Expiration Date Nurtec® ODT (rimegepant) 75mg 8-Unit Dose blister pack 72618-3000-2 All dates through 6/2026
CGMP Deviations
CGMP Deviations
Labeling; Incorrect NDC number on outer carton of product.
CGMP Deviations
CGMP Deviations
CGMP Deviations: Detection of N-nitroso-dabigatran (NDAB) impurity levels above the Acceptable Daily Intake Limit.
CGMP Deviations: Detection of N-nitroso-dabigatran (NDAB) impurity levels above the Acceptable Daily Intake Limit.
CGMP Deviations: Discoloration
Microbial Contamination of Non-Sterile Product: Objectionable organism, identified as Bacillus cereus, found in product during testing of repackaged product.
Defective Delivery System: Out of specification for shear.
Defective Delivery System: Out of specification for shear.
Defective Delivery System: Out of specification for shear.
Defective Delivery System: Out of specification for shear.