Olympus Corporation of the Americas: Medical Device Recall in 2020 - (Recall #: Z-1763-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Olympus Pleuravideoscope, Model LTF-240

Product Classification:

Class II

Date Initiated: March 23, 2020

Date Posted: April 29, 2020

Recall Number: Z-1763-2020

Event ID: 85208

Reason for Recall:

There was no data to validate that the identified endo-therapy devices were compatible with certain pleuravideoscope models. Updated Operations Manuals are being provided.

Status: Terminated

Product Quantity: 265 total

Code Information:

All Serial numbers

Distribution Pattern:

US Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated