Exact FDA event identifier

Event 90807

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket: July 27, 2022
Product types: Device
Classifications: Class II
Statuses: Ongoing
Recalling firm wording: BARCO NV

Dossier provenance

Source snapshots represented here

openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 1

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

Z-1854-2022

Recall number: Z-1854-2022
Initiated: July 27, 2022
Classification: Class II
Status: Ongoing
Recalling firm: BARCO NV
Quantity: 169 devices

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

installation issues

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

installation issues

Code information

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

Distribution pattern

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