Reported Mar 18, 2020 · Terminated
GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03
Verathon, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Verathon, Inc. · 20001 N Creek Pkwy · Bothell, WA · 98011-8218
Is this the product you have?
- GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03
- Lot codes and dates
- 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 ADomestic and Foreign Consignee List (in Associated Documents)
- Amount recalled
- 239 manuals
Where it was sold
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
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