PlainRecalls
ModerateClass IITerminated

FDA Devices recall · Reported November 11, 2015

Surgical Display, Model No. MDSC-2224 (24 inch), Model No. MDSC-2226 (26 inch) and Model No. MDSC-2242 (42 inch)

User settings were no longer on the monitor's memory after these systems were powered off and back on.

Recall #
Z-0227-2016
Affected scope
462 devices in US
Initiated
May 28, 2015
Compiled from official public sources by the editorial team.
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Barco Inc. recalled Surgical Display, Model No. MDSC-2224 (24 inch), Model No. MDSC-2226 (26 inch) and Model … - a moderate-severity action.

Surgical Display, Model No. MDSC-2224 (24 inch), Model No. MDSC-2226 (26 inch) and Model … was recalled by Barco Inc. in November 11, 2015. Reason: User settings were no longer on the monitor's memory after these systems were powered off and back on.. Check the official notice for the remedy. Verify recall #Z-0227-2016 with the FDA Devices before acting.

The recall

Barco Inc. issued this moderate-severity FDA Devices recall-User settings were no longer on the monitor's memory after these systems were powered off and back on..

Moderate
severity level
462 units
affected scope
Class II
classification
November 11, 2015
reported

Sourced from official FDA Devices enforcement records. Verify recall #Z-0227-2016 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Devices action (record #Z-0227-2016) was formally reported on November 11, 2015, with the manufacturer initiating the action on May 28, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. Barco Inc. is listed as the recalling firm, operating out of Duluth, GA. Federal records list the affected scope as 462 devices in US.

The documented reason for this recall is: User settings were no longer on the monitor's memory after these systems were powered off and back on. Distribution data in the federal record shows the product reached: US Distribution to the states of : AZ, CA, FL, GA, IL, MA, NE, NJ, OH, OR and TX., and Internationally to Canada.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Medical Devices recalls over time

Where this recall sits in its category - 40,322 medical devices recalls on record

-1,00001,0002,0003,0004,000 20052008201120142017202020232026 1,248
Severity2487872426High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Severity

Moderate

Affected scope

462 devices in US

Related Recalls

6

3 from same agency

Product description

Surgical Display, Model No. MDSC-2224 (24 inch), Model No. MDSC-2226 (26 inch) and Model No. MDSC-2242 (42 inch)

Reason for recall

User settings were no longer on the monitor's memory after these systems were powered off and back on.

Recall Profile

Structured summary of the FDA Devices recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Terminated
Recall number Z-0227-2016
Date reported November 11, 2015
Date initiated May 28, 2015
Recalling firm Barco Inc.
Firm location Duluth, GA
Affected scope 462 devices in US
Distribution US Distribution to the states of : AZ, CA, FL, GA, IL, MA, NE, NJ, OH, OR and TX., and Internationally to Canada.

Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

462 devices in US units affected - limited or regional distribution scale.

Regional (<10K units) ✓ This recall
Multi-state (10K – 100K units) -
Large-scale (100K – 1M units) -
Massive (≥1M units) -

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (Z-0227-2016) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Devices before acting, recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
Surgical Display, Model No. MDSC-2224 (24 inch), Model No. MDSC-2226 (26 inch) and Model No. MDSC-2242 (42 inch). Recalled by Barco Inc.. Units affected: 462 devices in US.
Why was this product recalled?
User settings were no longer on the monitor's memory after these systems were powered off and back on.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 11, 2015. Severity: Moderate. Recall number: Z-0227-2016.
Where was the recalled product distributed?
Distribution: US Distribution to the states of : AZ, CA, FL, GA, IL, MA, NE, NJ, OH, OR and TX., and Internationally to Canada..
How do I check if my product is affected by a recall?
Check the product description and recall number (Z-0227-2016) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device?
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

Nearby Recalls in This Category

Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.

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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported November 11, 2015. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.