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Open, Classified

i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngoscopy.

FDA Recall Z-2102-2025 · Posted 2025-07-11

Recalling FirmIntersurgical Inc
Recall StatusOpen, Classified
Product CodeCCW
Date Initiated2025-06-17
Product Quantity2,152 pieces

Reason for Recall

Potential for faulty devices as a result of depleted batteries.

Firm Action

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.

Root Cause

Component design/selection

Distribution Pattern

US distribution AZ, CA, FL, GA, IL, IN, KS, MD, MI, MO, NV, NY, OH, PA, SC, TX, VA.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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