Class I

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

Intersurgical Inc · June 17, 2025

Reason for Recall

Potential for faulty devices as a result of depleted batteries.

Distribution

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

States Affected

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

Quantity Affected

2,152 pieces

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2102-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.