The Triad Group alcohol prep pads are co-packaged
and distributed with Genentech medicines
Boniva Injection, Fuzeon, Nutropin A.Q. Pen, Pegasys, and TNKaseto customers in the United States.
According to the Food and Drug Administration's (FDA) Medwatch communication, the recall was initiated due to concerns about potential contamination of the Triad Group's products with the bacteria, Bacillus cereus. This recall involves those products marked as sterile as well as non-sterile.