Barco N.V.

Complete recall history across all FDA and CPSC categories — 5 total recalls

Barco N.V. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (5)

FDA medical device enforcement actions by Barco N.V.

Date Product Reason Class
May 9, 2025 Model: Description/REF: MNA-420: MNA-420 ENC -H/K9303320, MNA-420 DEC -H V2/K... Cathode ray tube display system encoders and decoders have same MAC address; ... Class II
Apr 24, 2024 MNA-420 ENC HDMI, Material Number K9303311; cathode ray tube display We have identified a potential issue with the SFP+ module supplied by Molex (... Class II
Dec 20, 2023 Barco MDSC-8527 NXF, Part Number K9352421 Barco became aware of a problem with I2C cables in the manufacturing process ... Class II
Jan 22, 2021 Barco MDNC-3421 DISPLAY, DIAGNOSTIC RADIOLOGY A number of MDNC-3421 displays were shipped while not being DICOM-compliant. ... Class II
Mar 30, 2017 Optional MDRC-1119 Front Cover Attachment Kit for review display monitors. ... If metal strips are removed and re-applied to another display, there is poten... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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