RecallRadar

FDA Device recall Z-0010-2018

iVue 500 with iScan, D216606

On 2017-09-06 the FDA classified a Class II recall of iVue 500 with iScan, D216606 by Optovue, citing FDA determined that a 510(k) is needed for the Vault Mapping software (also known as Lens Fitting).

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0010-2018
ClassificationClass II
Statusterminated
Initiated2017-07-27
Published2017-09-06
Last updated2026-09-13 11:54 UTC
CompanyOptovue
DistributionUS

Product

iVue 500 with iScan, D216606. Product non-contact, high resolution tomographic imaging device. It is intended for in vivo imaging, axial cross-sectional and three-dimensional imaging and measurement of anterior and posterior ocular structures, including retina, retinal nerve fiber layer, ganglion cell complex (GCC), optic disc, cornea, and anterior chamber of the eye. The iVue 500 with normative database is a quantitative tool for the comparison of retina, retinal nerve fiber layer, ganglion cell complex, and optic disc measurements to a database of known normal subjects. The iVue 500 with normative database is indicated for use as a device to aid in the diagnosis, documentation, and management of ocular health and diseases in the adult population.

Reason

FDA determined that a 510(k) is needed for the Vault Mapping software (also known as Lens Fitting).

Identifiers

code_infoCat No. 700-49428-001 (GTIN - N/A), 700-49428-002 (GTIN 00858848006315), 700-49428-003 (GTIN 00858848006018).

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0010-2018%22

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