FDA Drug Recalls

Recalls / Firms / Merck & Co. Inc

Merck & Co. Inc

5 FDA drug recalls on record.

DateClassDrugStatus
2025-07-21Class IIBelsomraOngoing
2014-01-13Class IIILiptruzet (ezetimibe and atorvastin) tablets,10 mg/20 mg, a) 30 count blister (NDC 6658Terminated
2014-01-13Class IIILiptruzet (ezetimibe and atorvastin) tablets,10 mg/10 mg, a) 30 count blister (NDC 6658Terminated
2014-01-13Class IIILiptruzet (ezetimibe and atorvastin) tablets,10 mg/80 mg, a) 30 count blister (NDC 6658Terminated
2014-01-13Class IIILiptruzet (ezetimibe and atorvastin) tablets,10 mg/40 mg, a) 30 count blister (NDC 6658Terminated