HIGH

Spacelabs Healthcare DVI Display Cables Recalled for EMI Risk in 2025 (012-0895-12, 820 Units)

Spacelabs Healthcare has recalled 820 DVI display cables worldwide due to shielding issues that may cause electromagnetic interference with other medical devices. The cables connect monitors used in patient care. Hospitals should stop using the affected cables and follow manufacturer recall instructions. The recall was issued by letter and is active as of 2025.

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

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

About This Product

These are external display cables used to connect monitors in clinical settings. They are part of patient-monitoring infrastructure.

Why This Is Dangerous

Shielding deficiencies can cause EMI that may affect nearby medical devices, potentially compromising patient safety.

Industry Context

This recall is not described as part of a broader industry pattern in the provided data.

Real-World Impact

Hospitals and clinics may need to replace these cables to prevent possible device interference. No injuries are reported in the data.

Practical Guidance

How to identify if yours is affected

  1. Identify model 012-0895-12 and confirm 12-foot DVI-I to DVI-I cable.
  2. Confirm usage with monitors 91390 and 91393.
  3. Check for the recall notice from Spacelabs Healthcare.

Where to find product info

FDA enforcement page for Z-0168-2026 and Spacelabs recall notice.

What timeline to expect

Replacement or refund timeline not specified; expect manufacturer guidance by letter.

If the manufacturer is unresponsive

  • Escalate to hospital safety office or regulatory body.
  • File a consumer incident report with FDA if needed.

How to prevent similar issues

  • In future purchases, require shielded, EMI-compliant cables.
  • Verify regulatory compliance marks (FDA approval) for medical accessories.
  • Keep records of all recall communications and purchase details.

Documentation advice

Keep the recall letter, product photos, model numbers, and purchase receipts for any refunds or replacements.

Product Details

Model/Catalog Number: 012-0895-12. Description: 12 foot DVI-I to DVI-I display cable. Used with monitors 91390 and 91393. Classification: Class II. Quantity: 820. Distribution: Worldwide, including all U.S. states and numerous countries. Brand: Spacelabs Healthcare.

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • 820 units recalled
  • Product: 012-0895-12, 12 ft DVI-I to DVI-I cables
  • Used with monitors 91390 and 91393
  • Global distribution including all US states
  • EMI shielding defect linked to patient-safety risk
  • Recall number Z-0168-2026; recall date 2025-09-05

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

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

Product Details

Model Numbers
012-0895-12
(01)10841522131479 (Xprezzon)
(01)10841522131455 (Qube)
UDI-DI for products that are used with the display cables. (01)10841522131479 (Xprezzon)
Affected States
ALL
Report Date
October 22, 2025
Recall Status
ACTIVE

Related Recalls

Vehicles & Parts
HIGH

Mazda CX-70 Recall 2025 for Powertrain Control Module Software May Lose Drive Power

Mazda North American Operations is recalling 2024 CX-90 and 2025 CX-70 SUVs sold through Mazda dealers. The PCM and ECM software can illuminate malfunction indicator lights and cause a loss of drive power, increasing crash risk. Owner notification letters were mailed December 19, 2024, and Mazda will reprogram the PCM and ECM at no charge.

Mazda
Loss of
Read more
Vehicles & Parts
HIGH

Nissan Kicks 2025 Certification Label Recall for GVWR/GAWR Errors (PD136, PMA47)

Nissan North America is recalling certain 2025 Nissan Kicks vehicles sold through Nissan dealers nationwide. The certification label may print incorrect GVWR and GAWR values, risking overload. Some SR trims with a 19-inch wheel package may display an incorrect wheel size on the label, and owners should contact their Nissan dealer to arrange replacement labels.

Nissan
An overloaded
Read more