36 FDA recalls mention Fluocinolone. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Fluocinolone.
Reason Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Reason Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Reason Failed Content Uniformity Specifications; at the 18 month time point.
Reason Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Reason Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Reason Subpotent Drug: the active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Reason Subpotent; 22 month stability timepoint
Reason Subpotent; 12 month stability timepoint
Reason Subpotent; fluocinolone acetonide.
Reason Subpotent; fluocinolone acetonide
Reason Subpotent; fluocinolone acetonide
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