Devices

Device Recall GlideScope Titanium SingleUse Video Laryngoscope

Model / Serial
LOT Number ranges: -LoPro S3: 081814 - 093015; -LoPro S4: 081114 - 090315; -MAC S3: 080814 - 101315; -MAC S4: 022514 - 082115;
Product Classification
Anesthesiology Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide Distribution - US (nationwide) and to countries of: Australia, Belgium, Canada, Denmark, France, Germany, Hong Kong, Italy, Luxembourg, Saudi Arabia, Singapore, Spain, Sweden, The Netherlands, U.A.E., and United Kingdom.
Product Description
GlideScope Titanium Single-Use Video Laryngoscope. It is a single-use video laryngoscope system (GlideScope Titanium System) consists of a sterile-packaged, single-use video laryngoscope, multi-use Smart Cable and portable GlideScope video monitor. || The system incorporates a high-resolution, full-color digital camera and monitor for real-time viewing and recording. || Affected Product Names and Part Numbers: || -LoPro S3: 0574-0130 (single blade) or 0270-0769 (box of 10) || -LoPro S4: 0574-0131 (single blade) or 0270-0770 (box of 10) || -MAC S3: 0574-0132 (single blade) or 0270-0771 (box of 10) || -MAC S4: 0574-0133 (single blade) or 0270-0772 (box of 10) || The GlideScope Video Laryngoscopes are intended for use by qualified medical professionals to obtain a clear, unobstructed view of the vocal cords for medical procedures.
Manufacturer
Verathon, Inc.
1 Event
- Recall of Device Recall GlideScope Titanium SingleUse Video Laryngoscope

Manufacturer

Verathon, Inc.

Manufacturer Address
Verathon, Inc., 20001 N Creek Pkwy, Bothell WA 98011-8218
Manufacturer Parent Company (2017)
Roper Technologies Inc
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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