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Subpotent Drug:Out of specification for percentage of active pharmaceutical ingredients.
1,590 recalls, newest first
Subpotent Drug:Out of specification for percentage of active pharmaceutical ingredients.
Subpotent Drug:Out of specification for percentage of active pharmaceutical ingredients.
Superpotent Drug: contains higher levels of Iron than labeled.
Failed dissolution specification -Two additional lots being recalled due to Out-of-Specification results observed for dissolution at 18th month stability testing.
Subpotent Drug: Isotretinoin content results were lower than the specification limit obtained during routing product monitoring.
GMP Deviations: Out of specification results for Total Aerobic Microbial count in excipient purified water sample
GMP Deviations: Out of specification results for Total Aerobic Microbial count in excipient purified water sample
GMP Deviations: Out of specification results for Total Aerobic Microbial count in excipient purified water sample
Superpotent Drug.
Sub-potent
Sub-potent
Presence of foreign tablet/capsule: A single foreign tablet was found in pharmacy dispensed bottle of 30 Estradiol 2 mg tablets.
Failed Impurities/Degradation Specifications:Out of specification for impurities.
Discoloration: This product is being recalled due to a confirmed pharmacist report that tablets from this lot were a pink color instead of cream (peach).
Labeling: Label Error on Declared Strength: Label incorrectly lists concentration as "10 mcg per mL" rather than the correct concentration of "100 mcg per mL".
Shortfill: Aprepitant capsules 40 mg is being recalled due to customer reports of missing capsule in the blister pack.
Superpotent Drug: recalled lots may have higher concentration of ibuprofen.
Superpotent Drug: recalled lots may have higher concentration of ibuprofen.
Superpotent Drug: recalled lots may have higher concentration of ibuprofen.
Incorrect excipient: Product was compounded in 250 mL 5% Dextrose instead of 250 mL 0.9% Sodium Chloride
Microbial Contamination of Non-Sterile Product: Presence of Pseudomonas aeruginosa in product
Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile.
cGMP violations noted during the firm's most recent inspection.
cGMP violations noted during the firm's most recent inspection.
cGMP violations noted during the firm's most recent inspection.