Recall Z-1854-2022— BARCO NV

Name: FDA recall Z-1854-2022
Creator: U.S. Food and Drug Administration
Published: 2022-07-27

Class II · Ongoing

Class II FDA medical device recall by BARCO NV, initiated 2022-07-27. It names one FDA 510(k) clearance: K173381. Product: Barco Medical Network Adapter, MNA-240, part of the NexxisOR system, Model Numbers: a) K9303078A, b) K9303097A. Reason: installation issues.

Recalling firm: BARCO NV
Classification: Class II
Status: Ongoing
Initiated: 2022-07-27
Firm location: Kortrijk, N/A, Bulgaria

510(k) clearances named in this recall

1 on FDA's record

K173381 — Nexxis ORBarco N.V.·cleared 2018-02-22

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

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

Reason for recall

installation issues

Data sourced from openFDA. This site is unofficial and independent of the FDA.