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Lower risk Medical device recall · FDA · Published December 20, 2023

Barco MDSC-8527 NXF Recall: I2C Cable Issue Blocks Decoder Function

Barco recalls limited batch of MDSC-8527 NXF units with defective I2C cables that block the built-in MNA decoder. Affected units have specific part numbers and UDI/DI codes.

🇺🇸 FDA recall #Z-0979-2024Medical deviceBarco ›
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Recalling firmBarco N.V.President Kennedypark 35 · Kortrijk, Belgium
✎ GovInfoNow plain-language explainer

Barco is recalling a limited batch of MDSC-8527 NXF products due to manufacturing defects in I2C cables that prevent the built-in MNA decoder from working. This issue affects specific units with the part number K9352421 and UDI/DI code 05415334043312. Read more at govinfonow.com/recall/56519-barco-mdsc-8527-nxf-recall-i2c-cable-issue-blocks-decoder.

Source Summary by GovInfoNow · govinfonow.com/recall/56519-barco-mdsc-8527-nxf-recall-i2c-cable-issue-blocks-decoder · Updated August 18, 2026 · FDA enforcement record: FDA #Z-0979-2024

Cite this page

“Barco MDSC-8527 NXF Recall: I2C Cable Issue Blocks Decoder Function.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/56519-barco-mdsc-8527-nxf-recall-i2c-cable-issue-blocks-decoder. Based on FDA recall #Z-0979-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0979-2024%22&limit=1).

The FDA announced on 2023-12-20 that Barco N.V. is recalling the Barco MDSC-8527 NXF due to a manufacturing defect in I2C cables that blocks the built-in MNA decoder functionality. The agency issued recall number Z-0979-2024 for this voluntary Class II action.

How to tell if you have it

  • Brand: Barco
  • Product: MDSC-8527 NXF
  • Part Number: K9352421
  • UDI/DI: 05415334043312
  • Quantity: 2 units

The hazard

The recall addresses a problem with I2C cables in the manufacturing process of a limited batch of MDSC-85xx NXF products. This defect causes the functionality of the built-in MNA decoder to be blocked.

Context

GovInfoNow's records show Barco N.V. has issued three other recalls since 2021-01-22, including a 2025-05-09 recall for Barco MNA-420/440/620/640 Encoders/Decoders where systems may disconnect due to shared MAC addresses. Other recent recalls of similar products include the 2024-04-24 Barco MNA-420 HDMI Display Recall regarding inaccessible HDMI channels and the 2021-01-22 Barco MDNC-3421 Display Recall for DICOM compliance issues. The FDA also recorded a 2025-12-05 recall for the Beaver-Visitec OME6000U Laser System involving USB cable manufacturing issues.

How to tell if you have this one

Check if your Barco MDSC-8527 NXF has the part number K9352421 and UDI/DI code 05415334043312. This specific batch was produced with a manufacturing defect in the I2C cables.

  • Brand
    Barco
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Verify your Barco MDSC-8527 NXF has the part number K9352421 and UDI/DI code 05415334043312.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “US Nationwide distribution in the state of New Jersey.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 56 days after the firm started it.

1. Firm started the recall: Dec 20, 202312. FDA classified it Class II: Feb 2, 202423. Published in FDA’s Enforcement Report: Feb 14, 2024320232024
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

Is there a risk of injury from this product?

The recall describes a functional issue but no safety hazards, so there is no risk of injury.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-0979-2024 (December 20, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0979-2024 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA