Olympus recalls Duravent Silicone Ventilation Tubes (model 240075) that may contain incorrect 1.32mm Tiny T Tubes instead of intended product. Consumers should check model numbers and lot numbers to verify.
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.
Olympus is recalling Duravent Silicone Ventilation Tubes (model 240075) because some units may contain the wrong 1.32mm Tiny T Tubes instead of the intended product. This could lead to incorrect usage or performance issues if the wrong tube is installed.
The recall involves potential incorrect product mix-up where Duravent Silicone Ventilation Tubes may contain 1.32mm Tiny T Tubes (model 70240076) instead of the intended product. This could lead to improper installation or function if the wrong tube is used.
Owners of Duravent Silicone Ventilation Tubes with model number 240075 are affected. Those using these tubes in ventilation systems may face incorrect product installation if the wrong model is present.
Check for model number 240075 on the tube. Look for lot numbers SM405666 or JB362646 and UDI codes starting with 00521925031883.
Verify the model number on the tube is 240075.
Check for lot numbers SM405666 or JB362646.
Olympus recalls Duravent Silicone Ventilation Tubes (model 240075) because some units may contain the incorrect 1.32mm Tiny T Tubes (model 70240076) instead of the intended product.
Check for model number 240075 and lot numbers SM405666 or JB362646 on the tube.
The recall does not specify a remedy, so no action is required if the product is correct.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0707-2025 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0707-2025 from Olympus. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
