GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03
Reported: March 18, 2020 Initiated: March 31, 2019 #Z-1471-2020
Product Description
GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03
Reason for Recall
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.
Details
- Recalling Firm
- Verathon, Inc.
- Units Affected
- 239 manuals
- Distribution
- 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
- Location
- Bothell, WA
Frequently Asked Questions
What product was recalled? ▼
GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03. Recalled by Verathon, Inc.. Units affected: 239 manuals.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 18, 2020. Severity: Moderate. Recall number: Z-1471-2020.
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