Gildess 1.5/30 (norethindrone acetate, 1.5 mg and ethinyl estradiol tablets, 0.03 mg, USP), 21 count, (a) 3 blisters (NDC…
Reason Subpotent Drug; Ethinyl Estradiol
296 FDA recalls mention Estradiol. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Estradiol.
Reason Subpotent Drug; Ethinyl Estradiol
Reason Superpotent and Subpotent drugs
Reason Superpotent and Subpotent drugs
Reason Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Reason Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Reason Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Reason Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Reason Lack of Assurance of Sterility
Reason Lack of Processing Controls
Reason Lack of Assurance of Sterility: Firm is recalling all unexpired lots of sterile compounded products after FDA inspection found concerns of lack of…
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility: The firm is recalling all sterile preparations within expiry due to deficient practices which may have an impact on…
Reason Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Reason Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Reason Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Reason Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Reason Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Reason Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Reason Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Reason Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Reason Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Reason Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Reason Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Reason Labeling: Incorrect or Missing Package Insert; Product is being recalled because the birth control packs were distributed with out-dated package…
Reason Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility
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