Alcon Research, LLC
1 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (1)
- Inspections (1)
Devices registered here (1)
- EndoilluminatorProduct code MPA (opens in a new tab) · Class II · Gastroenterology, Urology · 21 CFR 876.1500
Recalls & enforcement
- Class IITerminated2018-07-17Potential for the optical head to detach from the stand due to the lack of thread adhesive.
FDA inspections (1)
- NAI2016-01-21No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
Related
- All facilities operated by Alcon Laboratories, Inc.
- Alcon Canada (CA)
- Alcon Research, LLC (PA)
- Ciba Vision Asian Manufacturing and Logistics PTE, LTD (SG)
- CIBA VISION GMBH (DE)
- Alcon Research, LLC (CA)
- Alcon Research, LLC (GA)
- WAVELIGHT GmbH (DE)
- Alcon Research, LLC (TX)
- PT. CIBA VISION BATAM (ID)
- Alcon Research, LLC (CA)
- Alcon Research, LLC (WV)
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Alcon Research, LLC (FEI 1000117501) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1000117501-alcon-research-llc/
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