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
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Spacelabs Healthcare
- Product type
- DVI-I to DVI-I Display Cable
- 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)
- Sizes
- 12-foot
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
September 5, 2025
Reported by FDA DEVICE
October 22, 2025
RecallRadar source check
April 18, 2026
Consumer action
Use the official remedy and keep documentation.
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
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
- Identify model 012-0895-12 and confirm 12-foot DVI-I to DVI-I cable.
- Confirm usage with monitors 91390 and 91393.
- 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.
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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
- 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
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Safety Guide
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