Alcon Laboratories, Inc.
1 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (1)
Registered facilities (25)
- Alcon Canada FEI 3003228982 · CA
- Alcon Research, LLC FEI 2523835 · PA
- Ciba Vision Asian Manufacturing and Logistics PTE, LTD FEI 3017889743 · SG
- CIBA VISION GMBH FEI 3002806704 · DE
- Alcon Research, LLC FEI 3010208880 · CA
- Alcon Research, LLC FEI 1053053 · GA
- WAVELIGHT GmbH FEI 3002483854 · DE
- Alcon Research, LLC FEI 1000117501 · TX
- Alcon Research, LLC FEI 1610287 · TX
- PT. CIBA VISION BATAM FEI 3002807944 · ID
- Alcon Research, LLC FEI 1000125771 · CA
- Alcon Research, LLC FEI 3007530141 · WV
- Alcon Laboratories Belgium FEI 3015456951 · BE
- Alcon Research, LLC FEI 1119421 · WV
- WaveLight GmbH FEI 3010300699 · DE
- ALCON GRIESHABER AG FEI 3003398873 · CH
- WAVELIGHT GmbH FEI 3003288808 · DE
- ALCON GRIESHABER AG FEI 3033485955 · CH
- CIBA VISION JOHOR SDN.BHD., FEI 3006466212 · MY
- CIBA VISION ASIAN MANUFACTURING AND LOGISTICS Pte. Ltd. FEI 3003657720 · SG
- Alcon Vision, LLC FEI 3000215259 · MD
- OPTONOL, LTD FEI 3003701944 · IL
- LUMITHERA, INC. FEI 3016232028 · TX
- ALCON LABORATORIES IRELAND LTD. FEI 3002808262 · IE
- Alcon Research, LLC FEI 3013497605 · PA
Recalls & enforcement
- Class IITerminated2018-07-17Potential for the optical head to detach from the stand due to the lack of thread adhesive.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “Alcon Laboratories, Inc. — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-1610287-alcon-laboratories-inc/
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