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ALCON LABORATORIES IRELAND LTD.

IE Last updated 23 Oct 2026

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Devices
0
Registries
FDA
FDA recalls
1

Catalogue0

No devices listed yet from this manufacturer.

FDA recalls1

Recalls this firm reported to the FDA. Device pages show the recalls that name the device or the 510(k)/PMA it was cleared under.

  • 2022

    • 11 May 2022 Z-1269-2022 Class II Terminated Due to device (preloaded intraocular lens) mislabeling, associated with partial mixing of product during overlapping manufacturing runs, and attributed to improper manufacturing line clearance.

Information

Country
IE
Address
CORK BUSINESS AND TECHNOLOGY PARK, CORK Cork(City)
FDA FEI number
3002808262