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Invotec Dual Channel Electrode

INVOTEC INTERNATIONAL, INC. · Model 1 · UDI-DI 00818501020041

ETN
1
510(k) clearances
5,083
Adverse events (11 deaths)
31
Recalls
141
Facilities

Description

Invotec Dual Channel: The Laryngeal Surface Electrode is intended to be used as a disposable, self-adhesive electrode attached to an endotracheal tube and positioned for continuous EMG monitoring of the larynx during surgical procedures.

Recalls

DateFirmReason
2025-05-19Neurovision Medical Products IncProduct packaging contains the wrong part number and kit contents.
2025-02-24Checkpoint Surgical IncAdhesive on the back of the lead may not fully encapsulate the metallic portion of the wire and button subassembly, potentially leading to exposed metal. There is a risk of electri
2025-02-24Checkpoint Surgical IncAdhesive on the back of the lead may not fully encapsulate the metallic portion of the wire and button subassembly, potentially leading to exposed metal. There is a risk of electri
2024-07-25Technomed EuropeProduct has have presence of brown discoloration or substance on the hinge area of the device
2024-07-01Neurovision Medical Products Incmislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
2023-11-07Medtronic Xomed, Inc.Firm received reports of customers experiencing noise from the NIM System, lead-off or high impedance issues, or loss of/intermittent nerve monitoring,
2022-04-29Medtronic Xomed, Inc.The firm received reports of events related to airway obstruction while using NIM Standard Reinforced EMG Endotracheal Tubes & NIM CONTACT Reinforced EMG Endotracheal Tubes.
2022-04-29Medtronic Xomed, Inc.The firm received reports of events related to airway obstruction while using NIM Standard Reinforced EMG Endotracheal Tubes & NIM CONTACT Reinforced EMG Endotracheal Tubes.
2022-04-29Medtronic Xomed, Inc.The firm received reports of events related to airway obstruction while using NIM Standard Reinforced EMG Endotracheal Tubes & NIM CONTACT Reinforced EMG Endotracheal Tubes.
2021-12-22Medtronic Xomed, Inc.There is potential for multiple issues due to a manufacturing nonconformity.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.