FDAFDA · Food and drugs·Recall number D-1514-2014
Risperdal CONSTA (risperiDONE), 25 mg Dose Pack, Rx Only, Single Use Only Janssen Pharmaceuticals Inc., Titusville, NJ 08560 NDC 50458-306-11
Published August 13, 2014 · Recall initiated: September 11, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Non-Sterility: Janssen is recalling one lot of Risperdal CONSTA (risperiDONE) due to a sterility failure in a stability sample
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Brand
- RISPERDAL CONSTA
- Manufacturer
- Janssen Pharmaceuticals, Inc.
- Distributor
- Nationwide
- Lot
- Vial - 4212AAP1, Kit - 309316, Exp. 07/15
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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