# FDA recall Z-0707-2025

> **Olympus Corporation of the Americas** · Class II · device recall initiated 2024-11-19.

## Product

Duravent Silicone Ventilation Tube. Model Number: 240075.

## Reason for recall

Potential that Duravent Silicone Ventilation Tubes may contain incorrect product, specifically, 1.32 mm Tiny T Tubes (model: 70240076) instead of the intended Duravent Silicone Ventilation Tubes.

## Distribution

AL, AZ, CA, IL, KY, MD, MN, MO, NC, ND, NY, OK, PA, SC, TN, TX, WA, WI.  International distribution to Australia, Canada, Germany.

## Key facts

- **Recall number:** Z-0707-2025
- **Recalling firm:** Olympus Corporation of the Americas
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-11-19
- **Report date:** 2024-12-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Center Valley, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0707-2025

## Citation

> AI Analytics. FDA recall Z-0707-2025. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-0707-2025. Source: US FDA. Licensed CC0.

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