Levoxyl (levothyroxine sodium) tablets, USP 112 mcg, packaged in a) 100-count bottles (NDC 60793-855-01) and b) 1000-count…
Reason Chemical contamination: emission of strong odor after package was opened.
173 FDA recalls mention Levothyroxine. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Levothyroxine.
Reason Chemical contamination: emission of strong odor after package was opened.
Reason Chemical contamination: emission of strong odor after package was opened..
Reason Chemical contamination: emission of strong odor after package was opened..
Reason Chemical contamination: emission of strong odor after package was opened.
Reason Chemical contamination: emission of strong odor after package was opened.
Reason Chemical contamination: emission of strong odor after package was opened..
Reason Labeling: Error on Declared Strength. Product labeled to contain 150 mcg tablets actually contained 75 mcg tablets.
Reason Subpotent; 15 month stability (by mfr)
Reason Subpotent; 15 month stability
Reason Subpotent; 9-month stability interval
Reason Subpotent; 9-month stability interval
Reason Defective Container: A number of Synthroid bottles have a localized thin wall defect on the bottom which may potentially impact the stability of the…
Reason Defective Container: A number of Synthroid bottles have a localized thin wall defect on the bottom which may potentially impact the stability of the…
Reason Defective Container: A number of Synthroid bottles have a localized thin wall defect on the bottom which may potentially impact the stability of the…
Reason cGMP Deviations; does not meet in process specification requirements
Reason cGMP Deviations; does not meet in process specification requirements
Reason cGMP Deviations; does not meet in process specification requirements
Reason cGMP Deviations; does not meet in process specification requirements
Reason cGMP Deviations; does not meet in process specification requirements
Reason cGMP Deviations; does not meet in process specification requirements
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 Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.
Reason Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.
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