FDAClass IISeptember 4, 2019

EyeBOX recall

EyeBOX Model OCL 02

Why was EyeBOX recalled?

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

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Serial Numbers TT003, TT004, TT005

Product
EyeBOX Model OCL 02
Recalling firm
OCULOGICA
Quantity
3
Distribution
The products were distributed to the following US states: MD and NY
Recall date
September 4, 2019
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls