Class II · Moderate risk Terminated
Risperidone 1mg/Ml 30ml
Reason CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Risperdal CONSTA
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Non-Sterility: Janssen is recalling one lot of Risperdal CONSTA (risperiDONE) due to a sterility failure in a stability sample
What was recalled
Risperdal CONSTA (risperiDONE), 25 mg Dose Pack, Rx Only, Single Use Only Janssen Pharmaceuticals Inc., Titusville, NJ 08560 NDC 50458-306-11
- Recalling firm
- Janssen Pharmaceuticals, Inc.
- NDC code
- 50458-306-11
- Origin
- NJ, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-1514-2014
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Risperidone recalls
See all
Class II · Moderate risk Terminated
RisperiDONE Oral Solution
Reason cGMP Deviations: Potential product contamination with Burkholderia cepacia (B.cepacia) and Ralstonia pickettii (R. pickettii).
Class II · Moderate risk Terminated
RisperiDONE Oral Solution
Reason cGMP Deviations: Potential product contamination with Burkholderia cepacia (B.cepacia) and Ralstonia pickettii (R. pickettii).
Class III · Low risk Terminated
risperiDONE ORALLY DISINTEGRATING TABLETS
Reason Failed Impurities/Degradation Specifications: Out of specification for a known degradant.
Class III · Low risk Terminated
Risperidone Oral Solution
Reason Failed Impurities/Degradation Specifications: Out of Specification for an impurity at the 18 month stability time point.
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