FDA Reports

April 23, 2010

LIFEPAK 15 Defibrillator Recall

FDA notified healthcare professionals of a Class I recall of LIFEPAK 15 Monitor/Defibrillator manufactured and distributed between March 26, 2009 and December 15, 2009. There is […]
March 17, 2010

Tysabri Label Update

New safety information will be included in the Tysabri (natalizumab) drug label and patient Medication Guide: The risk of developing progressive multifocal leukoencephalopathy (PML) increases with […]
March 12, 2010

Baby Slings Can Cause Infant Suffocation

The U.S. Consumer Product Safety Commission (CPSC) is advising parents and caregivers to be cautious when using infant slings for babies younger than four months of […]
February 1, 2010

Depakote Spina Bifida Lawsuit

Depakote, a widely used anti-epileptic and anti-seizure drug, is manufactered and marketed by Abbott Laboratories. Depakote was first approved by the US FDA and introduced in the US […]
January 5, 2010

Trailblazer Support Catheter Class I Recall

Recall Class: Class I Date Recall Initiated: November 6, 2009 Product Name: Trailblazer Support Catheter Model Numbers Lot Numbers SC-014-135, SC-018-090,SC-035-065, SC-035-135,SC-014-150, SC-018-150,SC-035-090, SC-035-150. 7828282, 7792290, […]