Data Foundry

Medical device recalls 2012

The GlideScope Video Laryngoscope — Class I medical device recall Z-0478-2013

Terminated recall by Verathon, Inc., reported 2012-12-19, distributed nationwide. Re-usable video laryngoscope blades of the GlideScope GVL3, GVL4, and GVL5 were recalled due to potential crac

Recall numberZ-0478-2013
Product typeMedical device
ClassificationClass I
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmVerathon, Inc., Bothell, WA, United States
Recall initiated2012-10-25
Classified2012-12-07
Reported by FDA2012-12-19
Terminated2013-09-27
DistributedNationwide (US)
Countries outside the USAR, AU, CA, CN, DE, FR, GB, ID, JP, KR, NL, PA, PE, PH, PK, SG, TH, TW, VE
Quantity2,710 units
Reason classespackaging
Model numbers0574-0001, 0574-0007, 0574-0030

Product

The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that incorporates a high-resolution color camera, an LED light source, a rechargeable lithium battery, and video output to a remote monitor. It consists of a video laryngoscope and a portable video monitor. The affected GVL and Part numbers are GVL 3  0574-0007, GVL 4  0574-0001, and GVL 5  0574-0030. 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.

Reason for recall

Re-usable video laryngoscope blades of the GlideScope GVL3, GVL4, and GVL5 were recalled due to potential cracking.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0478-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.