Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GlideScope Video Laryngoscope Recalled by Verathon, Inc. Due to A typographical error in the Operations & Maintenance...
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, Operations & Maintenance Manual, 0900-4940 REV 03
Quantity: 239 manuals
Why Was This Recalled?
A typographical error in the Operations & Maintenance Manual incorrectly identifies the use of low level disinfection for the reusable video laryngoscope, specifically for the Titanium Blades.
Where Was This Sold?
This product was distributed to 33 states: AL, AZ, AR, CA, CO, CT, FL, GA, IL, KS, LA, MD, MI, MN, NE, NV, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SD, TN, TX, UT, VA, WA, WI
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