Duravent Silicone Ventilation Tube — Class II medical device recall Z-0707-2025
Ongoing recall by Olympus Corporation of the Americas, reported 2024-12-25, distributed in AL, AZ, CA, IL, KY, MD, MN, MO…. Potential that Duravent Silicone Ventilation Tubes may contain incorrect product, specifically, 1.32 mm Tiny T
| Recall number | Z-0707-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Olympus Corporation of the Americas, Center Valley, PA, United States |
| Recall initiated | 2024-11-19 |
| Classified | 2024-12-19 |
| Reported by FDA | 2024-12-25 |
| Distributed | AL, AZ, CA, IL, KY, MD, MN, MO, NC, ND, NY, OK, PA, SC, TN, TX, WA, WI |
| Countries outside the US | AU, CA, DE |
| Quantity | 984 units |
| Lot numbers | JB362646, SM405666 |
| Model numbers | 240075 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0707-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.