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Recall Observatory FDA recall evidence

Device product

Integre Pro Yellow LP561, Integre Pro Yellow LP6RY, Integre Pro Scan Green LP6G, Integre Pro Green LP5532 Spare, Optics Bench V2, L2G/LP6G

Z-1971-2023

March 16, 2023

Class II

Product summary

Firm
Ellex Medical Pty Ltd.
Event
Event 92532
Status
Ongoing
Classification
Class II
Quantity
57 systems in total (6 units shipped to United States)
Official record key
device-enforcement:Z-1971-2023

Official wording

Reason: When using a Laser-Indirect-Ophthalmoscope (LIO) as the delivery device, a scattered laser beam inside the laser cavity system may unintentionally exit through the Slit Lamp output port (SDS) and get emitted from the Objective Lens when the laser is fired.

Code information: Serial Nos., UDI IPY0374, (01) 0 9342395 00012 0 ISRY0242, (01) 0 9342395 00015 1 ISG0370, (01) 0 9342395 00024 3 IPG0539, (01) 0 9342395 00009 0 BG1190

Distribution pattern: US nationwide/ Worldwide Distribution

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    When using a Laser-Indirect-Ophthalmoscope (LIO) as the delivery device, a scattered laser beam inside the laser cavity system may unintentionally exit through the Slit Lamp output port (SDS) and get emitted from the Objective Lens when the laser is fired.