RecallRadar

FDA Device recall Z-1471-2020

GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03

On 2020-03-18 the FDA classified a Class II recall of GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03 by Verathon, citing A typographical error in the Operations & Maintenance Manual incorrectly identifies the use of low level disinfection for the reusable video laryngoscope, specifically for the Tit….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1471-2020
ClassificationClass II
Statusterminated
Initiated2019-03-31
Published2020-03-18
Last updated2026-09-13 11:55 UTC
CompanyVerathon
DistributionAL, AR, AZ, CA, CO, CT, FL, GA, IL, KS, LA, MD, MI, MN, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SD, TN, TX, UT, VA, WA, WI

Product

GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03

Reason

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.

Identifiers

code_info
GlideScope Video Laryngoscope Operation and Maintenance Manual Catalog #: 0900-4940 Product can be further identifie…GlideScope Video Laryngoscope Operation and Maintenance Manual Catalog #: 0900-4940 Product can be further identified as In-Service USB 0901-0197 Affected Revision Rev. 00 distributed January 1, 2019 February 28, 2019 GlideScope Video Laryngoscope Product Serial Numbers are included in Appendix A: Domestic and Foreign Consignee List (in Associated Documents)

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1471-2020%22

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