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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Monitoring Devices

Spacelabs DVI Display Cables Recalled for Electromagnetic Interference Risk

Agency Publication Date: October 16, 2025
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Summary

Spacelabs Healthcare, Inc. is recalling 25,897 DVI display cables used as external components for Xprezzon (91390) and Qube (91393) patient monitors. These cables are inadequately shielded, which prevents them from complying with electromagnetic interference standards. This defect can cause the cables to interfere with other electronically sensitive medical devices being used nearby.

Risk

The inadequately shielded cables can emit electromagnetic signals that disrupt the operation of other life-saving or diagnostic medical equipment. This interference poses a serious risk to patient safety by potentially causing nearby devices to malfunction or provide incorrect readings.

What You Should Do

  1. This recall involves Spacelabs DVI-I to DVI-I male/male display cables used with Xprezzon (91390) and Qube (91393) patient monitors.
  2. Check your patient monitor accessories for cables with model numbers 012-0895-01 (6 foot), 012-0895-12 (12 foot), or 012-0893-01 (16 inch).
  3. Stop using the recalled display cables immediately.
  4. Contact Spacelabs Healthcare or your equipment distributor to arrange for the return, replacement, or correction of the affected cables.
  5. Call the FDA Consumer Complaint hotline at 1-888-463-6332 for more information.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: DVI display cables (6 foot)
Variants: 6 foot, DVI-I to DVI-I male/male
Model / REF:
012-0895-01
UDI:
10841522131479
10841522131455

External display cable used with Xprezzon (91390) and Qube (91393) monitors.

Product: DVI display cables (12 foot)
Variants: 12 foot, DVI-I to DVI-I male/male
Model / REF:
012-0895-12
UDI:
10841522131479
10841522131455

External display cable used with Xprezzon (91390) and Qube (91393) monitors.

Product: DVI display cables (16 inch)
Variants: 16 inch, DVI-I to DVI-I male/male
Model / REF:
012-0893-01
UDI:
10841522131479
10841522131455

External display cable used with Xprezzon (91390) and Qube (91393) monitors.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97616
Status: Active
Manufacturer: Spacelabs Healthcare, Inc.
Sold By: Spacelabs Healthcare, Inc.; Medical device distributors
Manufactured In: United States
Units Affected: 3 products (8179; 820; 16898)
Distributed To: Alaska, Alabama, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, Nebraska, New Hampshire, New Jersey, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Virginia, Washington, Wisconsin, Wyoming

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.