Tracheal Intubation Fiberscope OLYMPUS LF-P- To be used with an Olympus Light Source, documentation equipment, display monitor and other ancillary equipment for management of Endotracheal Tube
FDA Recall Z-2341-2023 · Posted 2023-08-04
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Recalling FirmOlympus Corporation of the Americas
Recall StatusOpen, Classified
Product CodeEOQ
Date Initiated2023-05-26
Product Quantity686 units
Reason for Recall
Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the LF-V and LF-P are no longer compatible endoscopes for reprocessing in the OERs.
The addendum highlights the following changes:
1. Removal of LF-V and LF-P as compatible with the OER
2. Change conditions for ETO gas sterilization from 12% EtO to 100% EtO
3. Removing the reusable cleaning brush for the manual cleaning. Single Use brushes
remain compatible
Firm Action
Olympus issued two Urgent: Medical Device Corrective Action letters:
(1) VISERA TRACHEAL INTUBATION VIDEOSCOPE OLYMPUS LF TYPE V (LF-V)
TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-P (LF-P)
(2)ENDOSCOPE REPROCESSOR Affected Models: OER-ProTM, OER-MiniTM and OER-EliteTM.
Letters states reason for recall, health risk and action to take:
Our records indicate that your facility has purchased one or more LF-V and LF-P scopes.
(1)Olympus requests you to take the following actions:
1. Ensure all personnel are completely knowledgeable and thoroughly trained on the
changes to the reprocessing instructions described in this letter.
2. If you are using OER for high level disinfection of your LF-V and LF-P, please transition
to another compatible method of reprocessing as soon as possible.
3. Locate and replace any on-hand copies of the LF-V and LF-P Instructions for Use with
the updated version. Obtain a copy of the updated IFU by accessing our Olympus
Connect website:
How to access the Instructions for Use
a) Log in to www.OlympusConnect.com
b) Select Product Support , then Instruction Manuals
c) Navigate to the document entitled LF-V Instruction Manual and LF-P
Instruction Manual
If you require additional information about the updated Instruction for use, or need
assistance with accessing Olympus Connect, please contact our Technical Assistance
Center (TAC) at 1-800-848-9024 (option 1). The TAC department can assist you in
answering questions on the new Instructions Manual and new steps.
4. If a Scope ID tag (MAJ-1545) is used with your LF-V and LF-P, please dispose of your
MAJ-1545 since the LF-V and LF-P cannot be used with OERs.
5. Complete the enclosed response form and return to our recall partner, Sedgwick, via
Email ([email protected]) or Fax (866-842-0470). For any questions about
the acknowledgement form, please call the Sedgwick team at 888-912-7350.
(2)Our records indicate that your facility has purchased one or more of the afore mentioned
endoscope
Root Cause
Labeling Change Control
Distribution Pattern
Nationwide
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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