FDA Device recall Z-1471-2020
GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03
- FDA Device
- Class II
- terminated
- Published 2020-03-18
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
| Agency | FDA Device |
|---|---|
| Recall number | Z-1471-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-03-31 |
| Published | 2020-03-18 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Verathon |
| Distribution | AL, 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.
Other recalls by Verathon
- Brand Name: GlideScope Core 15-inch FHD Model/Catalog Number: 0570-0437 Software Version: Core 15 FHD v1.7 and earlier Product Description:…
FDA Device · Class II · 2024-06-12 · Verathon - Brand Name: GlideScope Core 15-inch Monitor Model/Catalog Number: 0570-0404 Product Description: Serialized Monitor
FDA Device · Class II · 2024-06-12 · Verathon - GlideScope Go Monitors
FDA Device · Class III · 2021-08-11 · Verathon - BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the bladder noninvasively
FDA Device · Class II · 2020-12-09 · Verathon - GlideScope Core OneTouch Smart Cable, REF: 0800 0601, an accessory to the GlideScope Video Laryngoscope System Per PLRA: The Core OneTouch…
FDA Device · Class I · 2020-07-15 · Verathon
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1471-2020%22
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