HIGH

Spacelabs Healthcare Recalls DVI Display Cables Over Safety Risk

Spacelabs Healthcare recalled 16,898 DVI display cables on September 5, 2025. The cables may not comply with electromagnetic interference standards, posing risks to patient safety. Healthcare providers and patients must 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 recalled product is a 16-inch DVI-I to DVI-I male/male display cable, Model Number 012-0893-01. These cables were distributed worldwide, including across the United States.

The Hazard

The cables may interfere with electronically sensitive medical devices due to inadequate shielding. This poses a serious risk to patient safety.

Reported Incidents

There are no specific incidents reported, but the potential for interference with medical devices raises significant safety concerns.

What to Do

Patients and healthcare providers should stop using the cables immediately. Contact Spacelabs Healthcare or your healthcare provider for further instructions.

Contact Information

For more information, contact Spacelabs Healthcare at their official website or via the recall notification letter.

Key Facts

  • Recall date: September 5, 2025
  • Quantity recalled: 16,898 units
  • Distribution: Worldwide including all U.S. states
  • Risk of interference with medical devices
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 Cable
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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