Comment
Author: Admin | 2025-04-28
88 MCGNDC Number: 00378180777 and 00378180710Lot Number(s): 8180781, 3191628, 3197139, 3188976, 3184929, and 3204909Expiration Date(s): 8/2025, 2/2025, 4/2025, 1/2025, 12/2024 and 8/2025What you should do:Do not continue to use LEVOTHYROXINE SODIUM 88 MCG if it has been recalledCheck your prescription label to see if you have any LEVOTHYROXINE SODIUM in the affected lot numbers and expiration dates.If you have the medication, contact the pharmacy that you received it from. Adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling 1-800-FDA-0178.LEVOTHYROXINE SODIUM 100 MCGOn 12/18/2024, Viatris manufacturer for Mylan recalled LEVOTHYROXINE SODIUM 100 MCG due to Superpotent Drug and Subpotent Drug: potency failures obtained. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.More information about the recall is at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.The detailed information of the recalled product is listed below:Recalled Drug: LEVOTHYROXINE SODIUM 100 MCGNDC Number: 00378180977 and 00378180910Lot Number(s): 8171269, 8179579, 3183815, 3189147,3192027, 3202894, 3192026, 3199781, 3192028 and 3202895Expiration Date(s): 2/2025, 7/2025, 11/2024, 1/2025, 2/2025, 7/2025, 2/2025, 6/2025, 2/2025 and 7/2025What you should do:Do not continue to use LEVOTHYROXINE SODIUM 100 MCG if it has been recalledCheck your prescription label to see if you have any LEVOTHYROXINE SODIUM in the affected lot numbers and expiration dates.If you have the medication, contact the pharmacy that you received it from. Adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling 1-800-FDA-0178.LEVOTHYROXINE SODIUM 112 MCGOn 12/18/2024, Viatris manufacturer for Mylan recalled LEVOTHYROXINE SODIUM 112 MCG due to Superpotent Drug and Subpotent Drug: potency failures obtained. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.More information about the recall is at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.The detailed information of the recalled product is listed below:Recalled Drug: LEVOTHYROXINE SODIUM 112 MCGNDC Number: 00378181110Lot Number(s): 8171623, 8164486, 3205462, 3192428 and 3184096Expiration Date(s): 2/2025, 11/2024, 8/2025, 2/2025 and 11/2024What you should do:Do not continue to use LEVOTHYROXINE SODIUM 112 MCG if it has been recalledCheck your prescription label to see if you have any LEVOTHYROXINE SODIUM in the affected lot numbers and expiration dates.If you have the medication, contact the pharmacy that you received it from. Adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling 1-800-FDA-0178.LEVOTHYROXINE SODIUM 125 MCGOn 12/18/2024, Viatris manufacturer for Mylan recalled LEVOTHYROXINE SODIUM 125 MCG due to Superpotent Drug and Subpotent Drug: potency failures obtained. The U.S.Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.More information about the recall is at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.The detailed information of the recalled product is listed below:Recalled Drug: LEVOTHYROXINE SODIUM 125 MCGNDC Number: 00378181377 and 00378181310Lot Number(s): 3182797, 8177587 and 3199816Expiration Date(s): 11/2024 and 6/2025What you should do:Do not continue to use LEVOTHYROXINE SODIUM 125 MCG if it has been recalledCheck your prescription label to see if you have any LEVOTHYROXINE SODIUM in the affected lot numbers and expiration dates.If you have the medication, contact the pharmacy
Add Comment