Notice: Get a jump on 2015 — Pay your 2015 ASA membership dues now!




January 23 - 25 2015, 12:00 AM - 12:00 AM


February 07 - 08 2015, 12:00 AM - 12:00 AM

ASA Certificate in Business Administration 2015

June 26 - 28 2015, 12:00 AM - 12:00 AM

Annual Perioperative Surgical Home Summit



December 18, 2014

0.9 Percent Sodium Chloride Injection USP in 100 mL MINI-BAG PLUS Container by Baxter: Recall - Particulate Matter


FDA MedWatch Recall - Particulate Matter

November 21, 2014

FDA MedWatch - Respironics California, Esprit V1000 and V200 Ventilators: Class I Recall - Power Failure May Occur


FDA MedWatch Respironics California Esprit V1000 and V200 Ventilators Class I Recall

November 21, 2014

FDA MedWatch - Highly Concentrated Potassium Chloride Injection, 10 mEq per 100 mL by Baxter: Recall - Mislabeled


Highly Concentrated Potassium Chloride Injection 10 mEq per 100 mL by Baxter Recall Mislabeled



Add this product to your shopping cart

Self-Education and Evaluation (SEE) Program

SKU: 30701-14CE

... Read more »

Single Copies, Member Price: $360

Verathon GlideScope Video Laryngoscope Reusable Blades: Class 1 Recall - Breaking Across the Tip of the Blade

Thursday, December 13, 2012

AUDIENCE: Anesthesiologists, Risk Managers

ISSUE: The GlideScope GVL Video Laryngoscope Resuable Blades are being recalled due to potential cracking and/or breaking across the tip of the blade, which potentially could result in pieces of the blade breaking off in a patient’s mouth and obstructing the airway or being swallowed, which may cause serious adverse health consequences, including death.

The affected GlideScope GVL blades are at risk of developing stress cracks at the blade tip that may not be readily visible during routine inspection prior to intubation.

BACKGROUND: 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. This product was manufactured from December 1, 2010 through August, 31, 2011 and distributed from December 14, 2010 through March 6, 2012.

RECOMMENDATION: Stop using the blades. Contact Verathon Customer Care to obtain replacement blades. Return the recalled blades back to Verathon.

Complete and return the Device Recall Notification Reply Form by fax to 1-425-883-2896 or by email at:

All returned products will be quarantined and destroyed later. Verathon will replace the affected video laryngoscope blades at no cost to customers. Customers in the U.S. and Canada with questions can call 1-800-331-2313. For customers located outside of the U.S. or Canada, please call 1-425-867-1348. Customer Care hours are: Monday through Friday, from 6:00am to 5:00pm Pacific Time for the U.S., and 6:00am to 4:30pm Pacific Time outside of the U.S. Customers may also email the company at

Read the complete MedWatch Safety Alert, including a link to the Recall Notice, at:

« Back to FDA Alerts and Recalls