International Medical Devices Database

Manufacturer Address
American Optisurgical Inc, 25501 Arctic Ocean Dr, Lake Forest CA 92630
Manufacturer Parent Company (2017)
American Optisurgical Inc
Source
USFDA
1 Event
- Recall of Device Recall Horizon

One device in the database

Device Recall Horizon

Model / Serial
Serial Numbers: 1114, 1116, 1118, 1120-1124, and 1126-1129.
Product Classification
Ophthalmic Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide distribution: USA (California), Brazil, Algeria, France, South Korea, India, and Peru.
Product Description
American Optisurgical, Horizon Phacoemulsification System, Model: HZN-2030, for ophthalmic surgery.

One manufacturer with a similar name

Learn more about the data here

American Optisurgical Inc

Manufacturer Address
American Optisurgical Inc, 26902 Vista Ter, Lake Forest CA 92630-8123
Source
USFDA

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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