Oculogica EyeBOX Model OCL 02 Recalled for Missing Precaution Statements
Oculogica is recalling three EyeBOX Model OCL 02 units because the user manual is missing two precaution statements.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 1/5 (Low).
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The recall is classified as Low severity because it involves a documentation issue (missing precaution statements) with no reported injuries or illnesses, fitting the rubric criteria for packaging or documentation-only problems.
Plain-English summary
Oculogica is recalling three units of the EyeBOX Model OCL 02. The recall was initiated after a review of the user manual revealed that two precaution statements were missing from the documentation.
The affected products are identified by serial numbers TT003, TT004, and TT005. These units were distributed to the states of Maryland and New York.
Consumers who possess these specific serial numbers should stop using the product and contact Oculogica for instructions on how to obtain the corrected user manual.
The recalled product
- Product
- EyeBOX Model OCL 02
- Manufacturer
- OCULOGICA
- Hazard
- Affected units
- 3
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- Serial Numbers TT003
- TT004
- TT005
Distribution
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