# FDA recall Z-2102-2025

> **Intersurgical Inc** · Class I · device recall initiated 2025-06-17.

## 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

- **Recall number:** Z-2102-2025
- **Recalling firm:** Intersurgical Inc
- **Classification:** Class I
- **Product type:** device
- **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

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

## Citation

> AI Analytics. FDA recall Z-2102-2025. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-2102-2025. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*