PHENYLephrine HCL in 0.9% Sodium Chloride injectable
Lack of assurance of sterility: Product bags leaking at seam.
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.
Lack of assurance of sterility: Product bags leaking at seam.
Lack of assurance of sterility: Product bags leaking at seam.
Lack of assurance of sterility: Product bags leaking at seam.
Lack of assurance of sterility: Product bags leaking at seam.
Lack of assurance of sterility: Product bags leaking at seam.
Lack of assurance of sterility: Product bags leaking at seam.
Lack of assurance of sterility: Product bags leaking at seam.
Lack of assurance of sterility: Product bags leaking at seam.
Lack of assurance of sterility: Product bags leaking at seam.
Lack of assurance of sterility: Product bags leaking at seam.
Presence of Foreign Substance: potential presence of plastic particles.
Failed Impurities/Degradation Specifications: Presence of an impurity peak that exceeds approved specification.
Contraceptive Tablets Out of Sequence- First 4 pills of the packet are brown, instead of the last four pills and the expiry/lot was not printed on the package.
Defective Delivery System: Elevated number of units with out of specification results for leak rate
Lack of assurance of sterility: customer complaints received for the presence of leaks.
Lack of assurance of sterility: customer complaints received for the presence of leaks.
GMP Deviations: The firm does not include an SOP for testing for out of specifications.
Failed Dissolution Specifications
Failed Dissolution Specifications
Failed Dissolution Specifications
Failed Impurities/Degradation Specifications; out of specification results for Sulphoxide Impurity and Total Impurities
Failed Stability Specifications: Out of Specification results obtained for preservative Methylparaben content.
Superpotent Drug: above specification for the assay.
PRESENCE OF FOREIGN TABLETS/CAPSULES: A 2.5 mg Amlodipine Besylate tablet was found co-mingled with 10 mg Amlodipine Besylate tablets in a bottle labeled as Amlodipine Besylate 10 mg.
Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplement: FDA analysis found the product to tainted with undeclared anabolic steroids and steroid like substances.