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 notified consignees and account executives via email on 06/17/2025. The notification instructed consignees and account executives to immediately discontinue use and quarantine any affected stock on hand, notify customers if affected units have been further distributed, and contact Intersurgical Customer Support at 800-828-9633 for a Return Goods Authorization (RGA) Number and return label to return all affected units. Also, they were instructed to complete and return the Customer Product Recall Acknowledgement Form.

• FDA enforcement recordOfficial FDA database entry for Z-2102-2025
• FDA device classification · CCWOfficial FDA classification for this device type
• CFR regulation · 21 CFR 868.5540The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find Intersurgical IncSearch for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.