PlainRecalls
FDA Devices Critical Class I Ongoing

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

Reported: July 23, 2025 Initiated: June 17, 2025 #Z-2102-2025

Product Description

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

Reason for Recall

Potential for faulty devices as a result of depleted batteries.

Details

Recalling Firm
Intersurgical Inc
Units Affected
2,152 pieces
Distribution
US distribution AZ, CA, FL, GA, IL, IN, KS, MD, MI, MO, NV, NY, OH, PA, SC, TX, VA.
Location
East Syracuse, NY

Frequently Asked Questions

What product was recalled?
i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngoscopy.. Recalled by Intersurgical Inc. Units affected: 2,152 pieces.
Why was this product recalled?
Potential for faulty devices as a result of depleted batteries.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 23, 2025. Severity: Critical. Recall number: Z-2102-2025.