Barco N.V. recalls Model: Description/REF: MNA-420: MNA-420 ENC -H/K9303320
Reason for recall
Cathode ray tube display system encoders and decoders have same MAC address; new system setup with two or more affected units can lead to systems not functioning reliably:audio, video and/or control signals might be interrupted or fall away, displays might switch to failover and back multiple times, devices/sources/sinks might not be discovered/available, might lead to delayed/prolonged procedures
Affected product
Check your device
Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.
Model: Description/2 codes
- MNA-420: MNA-420 ENC -H/K9303320
- MNA-420 DEC -H V2/K9303331
MNA-440: MNA-440 ENC -H/K9303300, MNA-440 DEC -H V2/K9303311
MNA-620: MNA-620 DEC -H/K9306210, MNA-620 ENC -H/K9306220
and MNA-640: MNA-640 DEC -H/K9306410, MNA-640 ENC -H/K9306420
components of the NexxisOR system
Lot / code information
- Serial #
K9303320/05415334002364/2531531598, 2531531604, 2531534397, 2531534420, 2531534430, 2531534466 — +208 moreShow all
K9303320/05415334002364/2531531598, 2531531604, 2531534397, 2531534420, 2531534430, 2531534466, 2531534905, 2531534948, 2531534956, 2531536564, 2531554560, 2531572616, 2531572628, 2531572634, 2531591962, 2531591973, 2531591992, 2531592064, 2531592096, 2531593814, 2531593818, 2531593823, 2531597597, 2531610546, 2531610547, 2531610572, 2531610578, 2531610580, 2531612404, 2531612420, 2531612424, 2531612430, 2531612431, 2531612432, 2531612433, 2531612434, 2531612436, 2531612442, 2531623109, 2531623114, 2531623131, 2531623133, 2531623141, 2531635578, 2531635582, 2531639224, 2531639261, 2531639263, 2531639353, 2531640594, 2531640597, 2531640598, 2531640603, 2531640626, 2531640634, 2531540640, 2531640646, 2531640658, 2531640660; K9303331/05415334026827/2531533275, 2531533289, 2531533292, 2531533293, 2531533304, 2531533310, 2531533312, 2531533314, 2531533316, 2531533353, 2531533356, 2531534284, 2531534292, 2531534362, 2531537718, 2531540799, 2531569738, 2531582287, 2531582290, 2531582311, 2531582315, 2531582378, 2531582750, 2531582755, 2531582790, 2531582791, 2531582826, 2531582827, 2531582829, 2531584018, 2531584044, 2531537696, 2531537726; K9303300/05415334002180/2531537815, 2531557845, 2531557866, 2531558588, 2531558727, 2531558738, 2531558753, 2531558754, 2531558759, 2531561761, 2531561785, 2531572541, 2531572557, 2531572568, 2531572576, 2531572847, 2531572862, 2531572872, 2531633606, 2531633662; K9303311/05415334026810/2531537674, 2531572141, 2531580810, 2531580935, 2531582319, 2531582331, 2531582341, 2531588386, 2531588401, 2531588404, 2531588456, 2531591560, 2531592036, 2531592037, 2531592046, 2531593872, 2531594457, 2531594475, 2531594481, 2531594503, 2531594515, 2531597664, 2531597713, 2531597717, 2531597726, 2531597795, 2531597806, 2531597809, 2531597810, 2531597820, 2531599836, 2531605356, 2531605390; K9306210/2531542260, 2531542263, 2531542270, 2531542292, 2531543553, 2531543568, 2531543588, 2531582676, 2531582691, 2531588558, 2531588562, 2531593741, 2531593749, 2531593752, 2531593763, 2531593764, 2531593768, 2531593777, 2531593784, 2531595829, 2531595831, 2531601786; K9306220/ 2531540107, 2531542441, 2531542470, 2531543538, 2531543549, 2531543611, 2531543613, 2531543640, 2531563132, 2531572740, 2531572759, 2531572770, 2531572814, 2531572827, 2531575652, 2531594331, 2531594332, 2531594336, 2531594348, 2531594350; K9306410/2531572228, 2531582713, 2531582724, 2531582725, 2531584168, 2531584176, 2531584191, 2531588591, 2531588593, 2531588598, 2531588616, 2531588626, 2531604519, 2531604535, 2531604544, 2531604545, 2531604549, 2531604550, 2531604551, 2531604593, 2531604637, 2531604649, 2531604658; K9306420/ 2531537844, 2531537870, 2531537889, 2531537901, 2531537902, 2531556037, 2531556043, 2531572419, 2531572433, 2531572440, 2531595759
What the firm is doing
On 5/9/2025, recall notices started being distributed to customers informing them of the following: 1) Assess & locate the non-installed affected units and contain them from further distribution. B) Assess & locate affected units that are installed at your customer side. Please make your customers aware of this notification. C) The impacted units will need to be sent back. Further information on the swaps will be provided in the coming days. D) Fill in and return the Acknowledgement Letter. If you don t have the Key Account Manager s contact details, or need other support, you can contact the firm 24/7 via their Support web page: https://www.barco.com/en/support
DistributionShow detailsHide
US Nationwide distribution in the states of TX, OH.
Use of the product may cause temporary or medically reversible adverse health consequences.
Sources & references
- FDA enforcement recordOfficial FDA database entry for Z-1994-2025
- FDA 510(k) clearance · K173381The device's official FDA premarket clearance record
- FDA device classification · DXJOfficial FDA classification for this device type
- CFR regulation · 21 CFR 870.2450The federal regulation governing this device
- FDA recall announcementSearch FDA.gov for the official press announcement
- Find Barco N.V.Search for the manufacturer's official notice
- News coverageRecent reporting on this recall and manufacturer
- openFDA data recordThe raw JSON record this page is built from
Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.
Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.
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