# FDA recall Z-1724-2025

> **Integra LifeSciences Corp. (NeuroSciences)** · Class II · device recall initiated 2025-04-04.

## Product

INSPIRA AIR BALLOON DILATION SYSTEM 10x40, 1 PK. Airway balloon dilation catheter.

## Reason for recall

Incorrect product packaged in INSPIRA AIR Balloon Dilation System carton.

## Distribution

US Nationwide distribution in the states of TX, MT, AL & OK.

## Key facts

- **Recall number:** Z-1724-2025
- **Recalling firm:** Integra LifeSciences Corp. (NeuroSciences)
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-04-04
- **Report date:** 2025-05-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Princeton, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1724-2025

## Citation

> AI Analytics. FDA recall Z-1724-2025. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-1724-2025. Source: US FDA. Licensed CC0.

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