Z-1854-2022 Class II Ongoing

Recalled by BARCO NV — Kortrijk, N/A

FDA device recall Z-1854-2022 was initiated by BARCO NV on July 27, 2022 and is designated Class II. Reason for recall: installation issues The recall status is ongoing. Affected quantity: 169 devices.

Recall Details

Product Type
Devices
Report Date
October 5, 2022
Initiation Date
July 27, 2022
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
169 devices

Product Description

Barco Medical Network Adapter, MNA-240, part of the NexxisOR system, Model Numbers: a) K9303078A, b) K9303097A

Reason for Recall

installation issues

Distribution Pattern

US Nationwide distribution in the states of FL, IL, NJ.

Code Information

a) K9303078A, UDI 05415334000056, all serial numbers; b) K9303097A, UDI 05415334001657, all serial numbers