S.P.Labs
Failed Stability Specifications
Every FDA drug recall initiated in 2024, newest first, with its risk class, status and the reason the FDA recorded. Use the cause and risk filters to narrow the year down.
557 recalls, newest first.
Failed Stability Specifications
Lack of Assurance of Sterility: Firm did not perform process validation.
Lack of Assurance of Sterility: Firm did not perform process validation.
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Failed Stability Specification: Water determination was found not complying with specification.
Failed Impurities/Degradation Specifications: Out of specification for organic impurities
Failed Impurities/Degradation Specifications: Out of specification for organic impurities
Failed Dissolution Specifications
Defective Container: Out of specification for weight due to a slow leakage at the 12-month stability timepoint.
Defective Container: Out of specification for weight due to a slow leakage at the 12-month stability timepoint.
Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.
Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.
Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.