The United States Food and Drug Administration (FDA) posted a Firm Press Release concerning GlideScope GVL Video Laryngoscope Reusable Blades, manufactured by Verathon Inc.
The manufacturer initiated a voluntary recall of GlideScope GVL Video Laryngoscopes reusable blades that were manufactured between December 2010 and August 2011. The recall includes the following models within the specified serial number ranges: GlideScope GVL 3, 0574-0007: MD10500 to MD112387; GlideScope GVL 4, 0574-0001: LG105000 to LG112758 and GlideScope GVL 5, 0574-0030: XL105000 to XL111798.
The firm voluntarily recalled the products after learning about design characteristics leading to cracked and broken blades. These laryngoscope blades have been found to be prone to developing cracks and/or breaking across the tip of the blade, which potentially could result in pieces of the blade breaking off in patient's mouths and obstructing the airway or being swallowed.
The manufacturer suggests healthcare facilities that have GlideScope GVL recalling reusable blades to stop using the blades and contact Verathon Customer Care to obtain a replacement blade.
For details, please refer to the following FDA website: http://www.fda.gov/Safety/Recalls/ucm330305.htm.
If you are in possession of the affected product, please contact your supplier for necessary actions.
Posted on 3 December 2012