OCULOGICA recalls EyeBOX Model OCL 02
- Recall date
- April 16, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2398-2019
- FDA classification
- Class II
- Brand / firm
- OCULOGICA
- Sold / distributed
- The products were distributed to the following US states: MD and NY
Why it was recalled
A review of the user manual revealed that two precaution statements were missing.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
EyeBOX Model OCL 02
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