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Janssen Pharmaceuticals, Inc.

Janssen Pharmaceuticals, Inc. Recalls

All product recalls associated with Janssen Pharmaceuticals, Inc..

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Oct 2018

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–4 of 4 recalls

Ortho-Novum 1/35 Tablets (Janssen) – Incorrect Dispenser Instructions (2018)

Labeling: Incorrect Instructions; Instructions included for use with the Veridate dispenser contained instructions for the Dialpak dispenser.

Class IIModerate

FDAOct 23, 2018Nationwide• Janssen Pharmaceuticals, Inc.

Ortho-Novum 7/7/7 Tablets (Janssen) – Incorrect Dispenser Instructions (2018)

Labeling: Incorrect Instructions; Instructions included for use with the Veridate dispenser contained instructions for the Dialpak dispenser.

Class IIModerate

FDAOct 23, 2018Nationwide• Janssen Pharmaceuticals, Inc.

Ortho-Cept Birth Control (Janssen) – Subpotent Medication (2015)

Subpotent Drug

Class II

Moderate

FDAApr 29, 2015Nationwide• Janssen Pharmaceuticals, Inc.

Risperdal CONSTA (Janssen) – Non-Sterility Risk (2013)

Non-Sterility: Janssen is recalling one lot of Risperdal CONSTA (risperiDONE) due to a sterility failure in a stability sample

Class IIModerate

FDASep 11, 2013Nationwide• Janssen Pharmaceuticals, Inc.