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Verathon, Inc. recalls GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03
Recalled March 18, 2020 · FDA recall Z-1471-2020 · Verathon
Hazard
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. · FDA Class II
Units
239 manuals
Sold at
US: RI, IL, FL, SD, NY, MD, CA, OH, LA, AZ, GA, WA, OK, NC, AL, PA, TN, NJ, NV, MI, OR, TX, NM, VA, UT, NE, WI, CO, AR, MN, CT, ND, and KS. OUS: Canada
Description
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.
Product
GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03
Manufacturer(s)
Verathon, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →