Janssen Pharmaceuticals recalls
Janssen Pharmaceuticals has 4 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 14 Nov 2018. The most frequent reason is sterility.
Total recalls4since 2014
Last 12 months0reported
Class I00% of total
Ongoing0latest 14 Nov 2018
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 4 100%Class III 0 0%
Why janssen pharmaceuticals is recalled
Product types
By year
All janssen pharmaceuticals recalls, newest first
4 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Ortho-Novum 7/7/7 (norethindrone/ethinyl/estradiol) Tablets recalled | Janssen Pharmaceuticals | Packaging Defects | Nationwide |
| Drug | CLASS II | Ortho-Novum 1/35 (norethindrone/ethinyl estradiol) Tablets recalled | Janssen Pharmaceuticals | Other | Nationwide |
| Drug | CLASS II | Ortho-Cept (0.15 mg desogestrel recalled by Janssen Pharmaceuticals | Janssen Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Risperdal Consta (risperiDONE), 25 mg Dose Pack recalledRisperdal Consta | Janssen Pharmaceuticals | Sterility | Nationwide |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.