FDA recall Z-2102-2025

Intersurgical Inc · Class I · device

Product

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.

Distribution

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

Key facts

Status
Ongoing
Initiation date
2025-06-17
Report date
2025-07-23
Voluntary/Mandated
Voluntary: Firm initiated
Location
East Syracuse, NY, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2102-2025