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

Recall date

June 17, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2102-2025

FDA classification

Class I

Brand / firm

Intersurgical Inc

Sold / distributed

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

Why it was recalled

Potential for faulty devices as a result of depleted batteries.

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

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