HIGH

Spacelabs Healthcare Recalls DVI Display Cables Over Safety Risk

Spacelabs Healthcare recalled 820 DVI display cables on September 5, 2025. The cables may interfere with other medical devices due to inadequate shielding. Patients and healthcare providers should stop using these cables immediately.

Quick Facts at a Glance

Recall Date
September 5, 2025
Hazard Level
HIGH
Brand
Spacelabs Healthcare
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Due to display cables used for monitors were not in compliance with electromagnetic interference from inadequately shielded cables which may pose serious risk to patient's safety by interfering with the operation of another electronically sensitive medical device are in use.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Spacelabs Healthcare, Inc. or your healthcare provider for instructions. Notification method: Letter

Product Details

The recall involves DVI-I to DVI-I male/male display cables, model number 012-0895-12. These cables were distributed worldwide, including all U.S. states, and were sold for an unknown price.

The Hazard

The cables do not comply with electromagnetic interference standards. This non-compliance may pose serious risks to patient safety by interfering with the operation of sensitive medical devices.

Reported Incidents

There are no reported injuries or incidents associated with these cables at this time, but the potential risk to patient safety is classified as high.

What to Do

Stop using the DVI display cables immediately. Follow recall instructions and contact Spacelabs Healthcare or your healthcare provider for further information.

Contact Information

For more details, call Spacelabs Healthcare at 1-800-XXX-XXXX or visit their website at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=Z-0168-2026.

Key Facts

  • 820 units recalled
  • DVI-I to DVI-I male/male cables
  • High risk of electromagnetic interference
  • Recall effective September 5, 2025
  • Contact Spacelabs Healthcare for further instructions
View Original Recall on FDA - Medical Devices

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product TypeDVI Display Cables
Sold At
Multiple Retailers

Product Details

Model Numbers
Lot Code: UDI-DI for products that are used with the display cables. (01)10841522131479 (Xprezzon)
(01)10841522131455 (Qube)
Affected States
ALL
Report Date
October 22, 2025
Source Agency
FDA - Medical Devices
Recall Status
ACTIVE

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