13 FDA recalls mention Desoximetasone. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Desoximetasone.
Reason cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Reason cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Reason cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Reason Failed Impurities/Degradation Specification; high out of specification results observed
Reason CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure…
Reason Superpotent Drug
Reason Failed Stability Specifications; out-of specification value for homogeneity / phase separation.
Reason Failed Stability Specifications: The subject lots exhibited OOS results for Homogeneity test (Moderate separation).
Reason Failed Stability Specifications: The subject lots exhibited OOS results for Homogeneity test (Moderate separation).
Reason Failed impurities/degradation specifications: product was out of specification for unknown impurity at the 9 month stability time point
Reason Subpotent Drug
Reason Failed Impurities/Degradation Specifications: Out of specification results for impurities testing was obtained at the 6 and 9 month time points.
Reason Penicillin Cross Contamination: All lots of all products repackaged and distributed between 01/05/12 and 02/12/15 are being recalled because they…
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