Johnson & Johnson Recalls 70,000 Invega Syringes
The Associated Press reports a unit of Johnson & Johnson has recalled 70,000 syringes of its antipsychotic drug Invega Sustenna after finding that some of the pre-filled syringes may have cracks which possibly could affect the drug''s sterility. Janssen, a unit of Johnson & Johnson, said in a letter to pharmacists and health care providers that the voluntary recall affects lots of its 234-milligram-strength injections. The crack is completely covered by the label and is not detectable by the user. The company said in the letter posted on its website that there have been no reports of adverse effects or infection since the product launched and no reports of leakage associated with cracked syringe barrels. No other strengths of the drug or products marketed by Janssen are affected. Invega was approved in December 2006 to treat schizophrenia. The drug is related to Risperdal, a former blockbuster antipsychotic that lost patent protection in 2008.