Olympus recalls Veran endobronchial models due to manufacturing defects affecting electromagnetic compatibility. These devices may interfere with other electronics. Consumers should contact Olympus for details.
Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic Navigation System, SPiN Planning Laptop Workstation, and all associated navigation instruments) manufacturing to design requirements and insufficient evidence to demonstrate adequate electromagnetic compatibility (EMC). EMC is the ability of electrical equipment and systems to function acceptably without interference and to not interfere with other devices within its operating environment
Olympus is recalling several endobronchial models including the INS-5500 View Optical Probe and SPiN Xtend 21ga. The devices have manufacturing issues that could cause electromagnetic interference, potentially disrupting medical equipment in use.
The Veran devices have manufacturing defects that affect electromagnetic compatibility. This means they might interfere with other medical equipment in the operating room, potentially causing malfunctions in critical systems.
Healthcare professionals using these Veran endobronchial models for medical procedures are most at risk. Patients using these devices during surgery may experience interference with other medical equipment.
Check for the model numbers listed: INS-5500 View Optical Probe, INS-5450 SPiN Xtend 21ga, INS-5440 View Peripheral Catheter, and others. All serial numbers and lot numbers are included in the recall.
Identify your Veran endobronchial model from the list of recalled items provided in the recall notice.
Reach out to Olympus Corporation of the Americas for specific instructions on how to address the issue.
The affected models include INS-5500 View Optical Probe, INS-5450 SPiN Xtend 21ga, INS-5440 View Peripheral Catheter, and others as listed in the recall notice.
The recall does not require immediate discontinuation; however, healthcare professionals should contact Olympus for specific guidance.
Check the model number and serial number against the list provided in the recall notice.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-2662-2023 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-2662-2023 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.
