Desoximetasone Ointment USP
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Most common reason: Stability / shelf life (7 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Desoximetasone. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Failed Impurities/Degradation Specification; high out of specification results observed
CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.
Superpotent Drug
Failed Stability Specifications; out-of specification value for homogeneity / phase separation.
Failed Stability Specifications: The subject lots exhibited OOS results for Homogeneity test (Moderate separation).
Failed Stability Specifications: The subject lots exhibited OOS results for Homogeneity test (Moderate separation).
Failed impurities/degradation specifications: product was out of specification for unknown impurity at the 9 month stability time point
Subpotent Drug
Failed Impurities/Degradation Specifications: Out of specification results for impurities testing was obtained at the 6 and 9 month time points.
Penicillin Cross Contamination: All lots of all products repackaged and distributed between 01/05/12 and 02/12/15 are being recalled because they were repackaged in a facility with penicillin products without adequate separation which could introduce the potential for cross contamination with penicillin.
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