Data Foundry

Medical device recalls 2020

GlideScope Core OneTouch Smart Cable — Class I medical device recall Z-2476-2020

Terminated recall by Verathon, Inc., reported 2020-07-15, distributed nationwide. When video laryngoscopy system users apply, twisting motions while connecting the blade in the HDMI port, or e

Recall numberZ-2476-2020
Product typeMedical device
ClassificationClass I
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmVerathon, Inc., Bothell, WA, United States
Recall initiated2020-06-05
Classified2020-07-09
Reported by FDA2020-07-15
Terminated2024-04-22
DistributedNationwide (US)
Countries outside the USAU, GB
Quantity437
Model numbers0601, 0800

Product

GlideScope Core OneTouch Smart Cable, REF: 0800 0601, an accessory to the GlideScope Video Laryngoscope System Per PLRA: The Core OneTouch Cables (Reusable Device) is ancillary equipment used with the Core 10 and Core 15 monitors. The monitor and workstation are intended to work with video endoscopes, in conjunction with ancillary equipment, for endoscopic procedures.

Reason for recall

When video laryngoscopy system users apply, twisting motions while connecting the blade in the HDMI port, or excessive torsion to the connection port, this force is transferred to the HDMI PCB, which may result in video synchronization interruption, loss of live image/blank screen, no cameras connected monitor warning, may present risk to patients, in which time to intubation is more critical.

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-2476-2020. 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.