The Centers for Disease Control and Prevention are investigation these reactions. All patients that were affected received propofol from 100 mL vials manufactured by Teva, according to the release.
Testing by the U.S. Food and Drug Administration found that the two lots, 31305429B and 31305430B, were positive for elevated levels of endotoxin.
Clinicians are advised to immediately stop using these lots of propofol from Teva while the CDC, FDA and Teva continue the investigation. To date, all case patients have recovered, according to the report.
Read the release about the Teva Pharmaceuticals propofol recall.
