Olymp: Olympus recalls Pleuravideoscope Model LTF-160 due to potential incompatibility with endo-therapy devices. Updated manuals provided. All serial numbers affected.
There was no data to validate that the identified endo-therapy devices were compatible with certain pleuravideoscope models. Updated Operations Manuals are being provided.
Olympus is recalling Pleuravideoscope Model LTF-160 devices because they may not be compatible with certain endo-therapy devices. This could lead to improper use if endo-therapy devices are used with the scope.
The recall states there was no data validating compatibility between the pleuravideoscope and certain endo-therapy devices. Using incompatible devices could lead to improper function or damage.
Medical professionals using Olympus Pleuravideoscope Model LTF-160 devices are affected. Those who use endo-therapy devices with this model are at higher risk.
Check for the model number LTF-160 on the device. All serial numbers are affected by this recall.
Olympus has provided updated operations manuals to address compatibility concerns.
Olympus recalls Pleuravideoscope Model LTF-160 due to no data validating compatibility with certain endo-therapy devices.
Olympus has provided updated operations manuals to address compatibility concerns. No immediate action is required beyond reviewing the updated manuals.
The recall indicates potential incompatibility with endo-therapy devices, which could lead to improper function. However, no specific safety risks are described in the record.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1762-2020 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1762-2020 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.