Recall Z-1471-2020— Verathon, Inc.
Class II · Terminated
Class II FDA medical device recall by Verathon, Inc., initiated 2019-03-31, terminated 2021-12-14. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Verathon, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2019-03-31
- Terminated
- 2021-12-14
- Firm location
- Bothell, WA, United States
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.