Severity
Critical
CriticalClass ITerminated
FDA Devices recall · Reported July 15, 2020
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.
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…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Verathon, Inc. recalled GlideScope Core OneTouch Smart Cable, REF: 0800 0601, an accessory to the GlideScope Vide… - a critical-severity action.
GlideScope Core OneTouch Smart Cable, REF: 0800 0601, an accessory to the GlideScope Vide… was recalled by Verathon, Inc. in July 15, 2020. Reason: When video laryngoscopy system users apply, twisting motions while connecting the blade in the HDMI port, or …. Check the official notice for the remedy. Verify recall #Z-2476-2020 with the FDA Devices before acting.
The recall
Verathon, Inc. issued this critical-severity FDA Devices recall-When video laryngoscopy system users apply, twisting motions while connecting the blade in the HDMI port, or ….
- Critical
- severity level
- 437 units
- affected scope
- Class I
- classification
- July 15, 2020
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2476-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2476-2020) was formally reported on July 15, 2020, with the manufacturer initiating the action on June 5, 2020. It is classified under Critical severity (Class I), with a current status of Terminated. Verathon, Inc. is listed as the recalling firm, operating out of Bothell, WA. Federal records list the affected scope as 437.
The documented reason for this recall is: 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… Distribution data in the federal record shows the product reached: Worldwide Distribution: US (nationwide) and countries of: Australia and United Kingdom.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
437
Related Recalls
6
3 from same agency
Product description
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | Z-2476-2020 |
| Date reported | July 15, 2020 |
| Date initiated | June 5, 2020 |
| Recalling firm | Verathon, Inc. |
| Firm location | Bothell, WA |
| Affected scope | 437 |
| Distribution | Worldwide Distribution: US (nationwide) and countries of: Australia and United Kingdom. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-2476-2020) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Verathon, Inc.. Units affected: 437.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 15, 2020. Severity: Critical. Recall number: Z-2476-2020.
Where was the recalled product distributed? ▼
Distribution: Worldwide Distribution: US (nationwide) and countries of: Australia and United Kingdom..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2476-2020) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported July 15, 2020. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.