Alcon Research, Ltd. recalls Alcon Monarch III (1) "C" Cartridge The device is used for implanting AcrySof intraocular lenses in the eye following c…
- Recall date
- September 5, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0978-2017
- FDA classification
- Class II
- Brand / firm
- Alcon Research, Ltd.
- Sold / distributed
- Distributed to Mexico only
Why it was recalled
The intraocular lens could become lodged within the cartridge
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Alcon Monarch III (1) "C" Cartridge The device is used for implanting AcrySof intraocular lenses in the eye following cataract removal
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