CVS Health Magnesium Citrate Saline Laxative Oral Solution DYE FREE Cherry Flavor
Microbial Contamination of Non-Sterile Products - Presence of Acetobacter nitrogenifigens bacteria
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Microbial Contamination of Non-Sterile Products - Presence of Acetobacter nitrogenifigens bacteria
Failed Impurities/Degradation Specifications
Failed Impurities/Degradation Specifications
Labeling: Wrong Barcode
Labeling: Label mix-up - ephedrine syringes mislabeled as phenylephrine.
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
Presence of Foreign Tablets: Pharmacist reported a tablet of baclofen in a bottle of 1000-count tramadol
Presence of Particulate Matter: Potential for black particulates in the drug product.
Defective Container: yellow-colored spike from cap lodged in the nozzle. Firm received several complaints from customers.
Failed Tablet/Capsule Specifications: There is a potential for the imprint, M 122, to be missing on some tablets.
Presence of Foreign Substance; Broken metal piece found embedded in tablet.
Presence of Foreign Substance: This oil based product may contain trace amounts of water for injection (WFI).
Presence of foreign substance: Product complaint of foreign material in reconstituted bottle.
Presence of foreign substance: Product complaint of foreign material in reconstituted bottle.
Discoloration: Dotted and yellow spots on tablets
Discoloration: Dotted and yellow spots on tablets
Subpotent drug
Lack of Assurance of Sterility: Complaints of syringe breakage
CGMP Deviation: Discontinuation of the Quality program by manufacturer that would assure product meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess.
CGMP Deviation: Discontinuation of the Quality program by manufacturer that would assure product meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess.
CGMP Deviation: Discontinuation of the Quality program by manufacturer that would assure product meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess.
Failed Release Testing: Out of specification for particulate matter test.
Marketed Without An Approved NDA/ANDA