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Nico Corp. recalls Myriad-LX Light Source-for delivery of light to the surgical field to enhance visualization of tissue during resection
Recalled June 16, 2021 · FDA recall Z-1840-2021 · Nico
Description
(1) Updated IFU for the LX Illumination Packs: Warning - Avoid contact between the distal opening of the delivery sleeve and tissue/debris within the surgical.field to prevent complete occlusion. Some surgical approaches (e.g., endonasal) may increase this potential. {f unintended reduction in light output occurs and/or occlusion of the sleeve is suspected, both the delivery sleeve and the fiber should be replaced (2) Removal for the LX Light Source potential for the distal tip of the sleeve/fiber assembly potential to burn healthy tissue resulting in minor to moderate injury to the patient or end user.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →