Morphine Sulfate Oral Solution
Defective container: Oral solution leaking from container.
Every FDA drug recall initiated in 2017, newest first, with its risk class, status and the reason the FDA recorded. Use the cause and risk filters to narrow the year down.
1,141 recalls, newest first.
Defective container: Oral solution leaking from container.
Lack of Sterility Assurance
Lack of Sterility Assurance
Lack of Sterility Assurance
Lack of Sterility Assurance
Microbial Contamination of Non Sterile Products; out of specification Total Plate Count
Superpotent Drug: high out-of-specification result for magnesium.
Presence of foreign substance: glass particle
Stability Data Does Not Support Expiry: lots do not have stability that supports the use of the container system.
Stability Data Does Not Support Expiry: lots do not have stability that supports the use of the container system.
Stability Data Does Not Support Expiry: lots do not have stability that supports the use of the container system.
Stability Data Does Not Support Expiry: lots do not have stability that supports the use of the container system.
Subpotent Drug: found to be below the specification for labeled assay.
Subpotent Drug: found to be below the specification for labeled assay.
Subpotent Drug: found to be below the specification for labeled assay.
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.
Marketed without an approved NDA/ANDA: product label states it contains anabolic steroids.
Marketed without an approved NDA/ANDA: product label states it contains anabolic steroids.
CGMP Deviations: Possibility of the presence of microbial contamination in the water used to manufacture this product lot.
Labeling: Label Mix-up: One bottle of Eliquis 5 mg tablet was found to contain lower-strength Eliquis 2.5 mg tablets only instead of the labeled 5 mg tablets.