FDA Medical Device Recalls (openFDA)
Olympus Corporation of the Americas: Olympus Pleuravideoscope, Model LTF-240
- Recall number
- Z-1763-2020
- Recalling firm
- Olympus Corporation of the Americas
- Product
- Olympus Pleuravideoscope, Model LTF-240
- Status
- Terminated
- Initiated
- 2020-03-23
- Posted
- not on file
- Terminated
- 2021-11-30
- Reason
- There was no data to validate that the identified endo-therapy devices were compatible with certain pleuravideoscope models. Updated Operations Manuals are being provided.
- Root cause
- Under Investigation by firm
- Action
- An Urgent Medical Device Correction notification letter dated 3/23/20 was sent to customers. Actions to be taken by the user: Our records indicate that your facility has purchased one or more of the above-referenced endoscopes. OLYMPUS requires that you take the following actions: a) Inspect your inventory of operation manuals for the referenced Olympus models and discard the existing ones. b) Exchange them with the updated, enclosed Operation Manuals having an updated system chart indicating compatible endoscope accessories. c) Notify related personnel at your institution that they should stop the combination use of the LTF-160 and LTF-240 and the subject Endo-Therapy accessories. d) Access the Olympus recall portal to indicate that you have received this notification. Go to https://olympusamerica.com/recall. Enter the recall number Recall-0066 and provide your contact information as indicated in the portal. e) If you have further distributed this product, identify your customers, forward them this notification including the attachments, and appropriately document your notification process. Olympus regrets any inconvenience caused and fully appreciates your prompt cooperation in addressing this situation. If you require additional information, please do not hesitate to contact me directly at (484)896-5688 from Monday till Friday 8AM ET to 5PM ET or by e-mail at laura.storms@olympus.com.
- Quantity
- 265 total
- Distribution
- US Nationwide
- Lot, serial or model codes
- All Serial numbers
- 510(k) numbers
- ["K013617"]
- PMA numbers
- not on file
- Product code
- GCJ
- Firm FEI
- 2429304
- Firm city
- Center Valley
- Firm state
- PA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28