Carl Zeiss Suzhou Co., Ltd.: Medical Device Recall in 2023 - (Recall #: Z-0183-2024)

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:

OPMI LUMERA 300, REF 6137

Product Classification:

Class II

Date Initiated: August 18, 2023

Date Posted: November 1, 2023

Recall Number: Z-0183-2024

Event ID: 93146

Reason for Recall:

Surgical microscope for use in ophthalmology may be missing a screw from the suspension arm, which may cause the suspended components to fall from the suspension arm, which may injure any person under the suspended components.

Status: Ongoing

Product Quantity: 8

Code Information:

UDI-DI/Serial Numbers: 06909262061375/6137104455, 6137104627, 6137104623, 6137104678, 6137104233, 6137104620, 6137104480, 6137104613

Distribution Pattern:

US Nationwide distribution in the states of MD, TX, CA, GA, LA.

Voluntary or Mandated:

Voluntary: Firm initiated