Class II

Medical Device Recall: Duravent Silicone Ventilation Tube. Model Number: 240075.

Olympus Corporation of the Americas · November 19, 2024

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.

States Affected

AL, AZ, CA, IL, KY, MD, MN, MO, NC, ND, NY, OK, PA, SC, TN, TX, WA, WI

Quantity Affected

984 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0707-2025

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.

Olympus Corporation of the Americas Medical Device Recall: Duravent Silicone Ventilation Tube. Model Number: 240075. | SafeCheck