Olympus Corporation of the Americas: Medical Device Recall in 2024 - (Recall #: Z-0707-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Duravent Silicone Ventilation Tube. Model Number: 240075.

Product Classification:

Class II

Date Initiated: November 19, 2024

Date Posted: December 25, 2024

Recall Number: Z-0707-2025

Event ID: 95716

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.

Status: Ongoing

Product Quantity: 984 units

Code Information:

Model Number: 240075. UDI: 00521925031883 (17)331015 (10)SM405666, Lot Number: SM405666. UDI: 00521925031883 (17)331015 (10)JB362646, Lot Number: JB362646.

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated