The Recall Desk
LowFDA (Devices)·Z-2398-2019·Announced 2019-09-04

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.

What this means for you

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
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

Distributed in 2 states: