Janssen Pharmaceuticals recalls
FDA enforcement reports naming Janssen Pharmaceuticals, Inc. as the recalling firm.
- Recall reports
- 4
- Class I (serious)
- 0
- Most recent report
- Nov 14, 2018
- Nov 14, 2018Ortho-Novum 1/35 (norethindrone/ethinyl estradiol) Tablets, 1 mg/0Drug · Janssen Pharmaceuticals, Inc.Labeling: Incorrect Instructions; Instructions included for use with the Veridate dispenser contained instructions for the Dialpak dispenser.Class II
- Nov 14, 2018Ortho-Novum 7/7/7 (norethindrone/ethinyl/estradiol) Tablets, 0Drug · Janssen Pharmaceuticals, Inc.Labeling: Incorrect Instructions; Instructions included for use with the Veridate dispenser contained instructions for the Dialpak dispenser.Class II
- May 20, 2015Ortho-Cept (0Drug · Janssen Pharmaceuticals, Inc.Subpotent DrugClass II
- Aug 13, 2014Risperdal CONSTA (risperiDONE), 25 mg Dose Pack, Rx Only, Single Use Only Janssen Pha…Drug · Janssen Pharmaceuticals, Inc.Non-Sterility: Janssen is recalling one lot of Risperdal CONSTA (risperiDONE) due to a sterility failure in a stability sampleClass II