FDA Drug Recalls

Recalls / Brands / Cardizem Cd

Cardizem Cd

4 FDA drug recalls involving brand “Cardizem Cd.

DateClassProductFirm
2019-01-30Class IIICardizem CD (diltiazem HCl) capsules, 120 mg, packaged in a) 30-count bottles (NDC 0187-0795-30); and b) 90-coValeant Pharmaceuticals North America LLC
2019-01-30Class IIICardizem CD (diltiazem HCl) capsules, 240 mg, packaged in a) 30-count bottles (NDC 0187-0797-30); and b) 90-coValeant Pharmaceuticals North America LLC
2019-01-30Class IIICardizem CD (diltiazem HCl) capsules, 300 mg, packaged in a) 30-count bottles (NDC 0187-0798-30); and b) 90-coValeant Pharmaceuticals North America LLC
2019-01-30Class IIICardizem CD (diltiazem HCl) capsules, 180 mg, packaged in a) 30-count bottles (NDC 0187-0796-30); and b) 90-coValeant Pharmaceuticals North America LLC