Recall database

Intersurgical Inc recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 1–3 of 3 recalls

Class IIOngoingZ-2276-2025

Intersurgical Inc recalls One-piece Guedel airway

Potential contamination with small burrs, which if detach could be inhaled and result in potential complications such as airway obstruction, tissue irritation, inflammation and infection.

Anesthesiology Oropharyngeal Airway
Process control

Intersurgical IncNYAug 13, 2025

Class IIOngoingZ-2275-2025

Intersurgical Inc recalls One-piece Guedel airway

Potential contamination with small burrs, which if detach could be inhaled and result in potential complications such as airway obstruction, tissue irritation, inflammation and infection.

Anesthesiology Oropharyngeal Airway
Process control

Intersurgical IncNYAug 13, 2025

Class IOngoingZ-2102-2025

Intersurgical Inc recalls i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is…

Potential for faulty devices as a result of depleted batteries.

Rigid Laryngoscope
Component design/selection

Intersurgical IncNYJul 23, 2025