Verathon recalls GlideScope Video Laryngoscope manual with incorrect low-level disinfection instructions for titanium blades. Affected units include specific revisions and serial numbers. Contact for correction.
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.
Verathon recalls a specific version of their GlideScope Video Laryngoscope due to an error in the maintenance manual that could lead to improper disinfection of titanium blades. This error might cause blades to become contaminated or damaged if users follow the incorrect instructions.
The manual incorrectly states that low-level disinfection is safe for titanium blades. In reality, titanium blades require high-level disinfection to prevent contamination and damage. This error could lead to improper cleaning and potential infection risks.
Healthcare professionals using the GlideScope Video Laryngoscope with the affected manual revision are most at risk. The recall applies to specific model versions sold between January 2019 and February 2019.
Check if your GlideScope Video Laryngoscope manual is version 0900-4940 REV 03. Affected units were sold between January 2019 and February 2019 with specific serial numbers listed in Appendix A of the manual.
Verify your GlideScope Video Laryngoscope manual version is 0900-4940 REV 03.
No, the recall does not require immediate discontinuation. The hazard is a manual error, not a product defect.
Check your manual version and serial numbers listed in Appendix A of the manual for affected units sold between January 2019 and February 2019.
The official recall does not specify a remedy. Contact Verathon directly for guidance on correcting the manual.
We’ve drafted a message you can send Verathon to request your refund or repair — edit it as you like.
Subject: Recall Z-1471-2020 — Verathon Verathon Hello, I own a Verathon that is covered by recall Z-1471-2020 from Verathon. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
