LX3 Floor Stand for Endure Luxite Envision Optical System — Class II medical device recall Z-2448-2015
Terminated recall by Alcon Research, Ltd., reported 2015-09-02, distributed nationwide. Alcon is initiating a voluntary recall of all LX3 Microscope Floor Stands after receiving reports concerning l
| Recall number | Z-2448-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Alcon Research, Ltd., Fort Worth, TX, United States |
| Recall initiated | 2015-08-11 |
| Classified | 2015-08-21 |
| Reported by FDA | 2015-09-02 |
| Terminated | 2016-11-04 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, AT, AU, BE, BG, CA, CH, CL, CN, CO, CR, CZ, DE, DK, DO, ES, FR, GB, GR, GT, HU, IN, IT, JO, JP, KR, LB, MX, MY, NZ, OM, PA, PH, PL, PT, QA, RO, SA, SG, SK, TH, TR, TW, UA, ZA |
| Quantity | 688 units |
| Serial numbers | 1402548501X, 1502857606X |
Product
LX3 Floor Stand for Endure Luxite Envision Optical System; Endure LuxOR Q-Vue. Product Usage: The LX3 Microscope Floor Stand is an accessory to the LuxOR Opthalmic Microscope and the LuxOR Opthalmic Microscope with Q-VUE 3-D Assistant Visualization and provides a portable suspension system for the microscope that integrates an AC power module and microscope controls (Primary Control Panel and connectivity of foot controllers)
Reason for recall
Alcon is initiating a voluntary recall of all LX3 Microscope Floor Stands after receiving reports concerning loss of functionality due to issues with the cabling between the power, host and illumination modules, potentially causing the system to display a system message, and/or resulting in illumination failure.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2448-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.