Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GlideScope Video Laryngoscope (GVL) Recalled by Verathon, Inc. Due to Certain models and serial numbers of GlideScope GVL...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Verathon, Inc. directly.
Affected Products
GlideScope Video Laryngoscope (GVL), Part Number GVL 3 - 0574-0007; GVL 4 - 0574-0001; GVL 5- 0574-0030. The system consists of a video laryngoscope and portable video monitor. The GlideScope Video Laryngoscopes are intended for use by qualified medical professionals to obtain a clear, unobstructed view of the vocal cords for medical procedures. GVL is a video laryngoscope that incorporates a high resolution color camera, an LED light source and video output to a remote monitor.
Quantity: total 612 units (394 units in the US and 218 units outside the US)
Why Was This Recalled?
Certain models and serial numbers of GlideScope GVL and AVL laryngoscope blades may separate, due to inadequate bonding of the silicone adhesive affixing the halves of the blade. The potential for blade separation may not be readily visible during routine inspection before or after intubation.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Verathon, Inc.
Verathon, Inc. has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report