More than 44,000 Vials of Procrit Recalled
Date Published: Wednesday, August 6th, 2008
Procrit is being recalled by Johnson & Johnson subsidiary Ortho Biotech. According to the company’s recall notice, the action is necessary because cracks in the necks of a small number of Procrit vials were discovered upon post-manufacturing inspection.
The Procrit recall involves approximately 44,292 vials of lot P114942A distributed between April 15, 2008 and July 17, 2008.