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 Failed Tablet/Capsule Specifications: This recall is being carried out due to an out of specification result for appearance.
Reason Chemical contamination: Firm's inspection discovered the presence of 2-phenylphenol in the product due to migration from the cardboard cartons in…
Reason Chemical contamination: Firm's inspection discovered the presence of 2-phenylphenol in the product due to migration from the cardboard cartons in…
Reason Chemical contamination: Firm's inspection discovered the presence of 2-phenylphenol in the product due to migration from the cardboard cartons in…
Reason Failed Tablet/Capsule Specification; tablet breakage while pushing through the blister pack (dispenser) .
Reason Tablet/Capsule Imprinted with Wrong ID; a portion of the tablets could contain the incorrect debossing on one side of the tablet U2 instead of U3.
Reason Failed Impurity/Degradation Specifications due to moisture ingress in individual bottles
Reason Failed Impurity/Degradation Specifications due to moisture ingress in individual bottles
Reason Impurities/Degradation Products: Out-of-specification results were obtained for a known impurities.
Reason Defective Container: Pump head detaching from the canister unit upon removal of the overcap.
Reason Cross Contamination With Other Products: The firm recalled Zovia, Lutera, Necon, and Zenchent, because certain lots could potentially be contaminated…
Reason Cross Contamination With Other Products: The firm recalled Zovia, Lutera, Necon, and Zenchent, because certain lots could potentially be contaminated…
Reason Cross Contamination With Other Products: The firm recalled Zovia, Lutera, Necon, and Zenchent, because certain lots could potentially be contaminated…
Reason Cross Contamination With Other Products: The firm recalled Zovia, Lutera, Necon, and Zenchent, because certain lots could potentially be contaminated…
Reason Cross Contamination With Other Products: The firm recalled Zovia, Lutera, Necon, and Zenchent, because certain lots could potentially be contaminated…
Reason Impurities/Degradation Products: High Out-of-specification results were obtained for both known and unknown impurities.
Reason Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all Sterile Human Drugs distributed between 11/21/2011 and 05/21/2012 because…
Reason Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all Sterile Human Drugs distributed between 11/21/2011 and 05/21/2012. FDA…
Reason Cross Contamination w/Other Products: This active pharmaceutical ingredient is being recalled due to cross contamination with another product.
Reason Impurities/Degradation: This recall is being carried out due to the potential for some lots not meeting impurity specifications.
Reason Contraceptive Tablets Out of Sequence: This recall has been initiated due to the potential that some regimen packages may not contain placebo tablets.
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