OCULOGICA: Medical Device Recall in 2019 - (Recall #: Z-2398-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

EyeBOX Model OCL 02

Product Classification:

Class II

Date Initiated: April 16, 2019

Date Posted: September 4, 2019

Recall Number: Z-2398-2019

Event ID: 82922

Reason for Recall:

A review of the user manual revealed that two precaution statements were missing.

Status: Terminated

Product Quantity: 3

Code Information:

Serial Numbers TT003, TT004, TT005

Distribution Pattern:

The products were distributed to the following US states: MD and NY

Voluntary or Mandated:

Voluntary: Firm initiated