Oculus Optikgeraete GMBH: Medical Device Recall in 2023 - (Recall #: Z-2483-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Oculus Pentacam AXL , Ref 70100, CE 0123

Product Classification:

Class II

Date Initiated: August 8, 2023

Date Posted: September 6, 2023

Recall Number: Z-2483-2023

Event ID: 92847

Reason for Recall:

Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.

Status: Ongoing

Product Quantity: 364 units

Code Information:

UDI-DI; (01) 04049584012333

Distribution Pattern:

US Nationwide distribution in the states of CA, FL, MA, MN, NY, NC, OH, PA, TX, VA, WA. OUS: Not Provided

Voluntary or Mandated:

Voluntary: Firm initiated