Exela Pharma Sciences recalls ibuprofen lysine injection vials
Exela Pharma Sciences, LLC voluntarily recalled a lot of its ibuprofen lysine injection vials after discovering some of the vials contained particulate matter.
The FDA announced the recall in a news release on Feb. 8.
Ibuprofen lysine injection is used to close a clinically significant patent ductus arteriosus in premature infants when medical management is ineffective.
Exela and marketer X-Gen Pharmaceuticals have received no adverse event reports related to the recall. However, the companies said that participate matter could block blood vessels, provoke an immune reaction and/or lead to potentially life threatening microinfarcts.