Class IIOngoingZ-2953-2026
Intersurgical Inc recalls One-Piece Guedel Airway
Devices could potentially be occluded or partially occluded.
Intersurgical IncNYAug 26, 2026
Intersurgical Inc recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–5 of 5 recalls
Class IIOngoingZ-2952-2026
Intersurgical Inc recalls One-Piece Guedel Airway
Devices could potentially be occluded or partially occluded.
Intersurgical IncNYAug 26, 2026
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.
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.
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.
Intersurgical IncNYJul 23, 2025