Spacelabs Healthcare recalls DVI display cables (model 012-0893-01) that may interfere with medical devices, posing serious patient safety risks. Affected units sold with 91390/91393 monitors.
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.
Spacelabs Healthcare is recalling DVI display cables that could interfere with medical devices, potentially causing patient safety risks. This recall affects cables sold with specific medical monitors.
The cables lack proper shielding, which can cause electromagnetic interference. This interference might disrupt the operation of other sensitive medical devices, risking patient safety.
Medical facility staff using the 91390 or 91393 monitors with these cables are most at risk. Patients using the connected medical devices may be affected.
Check for model number 012-0893-01 on the cable. These cables were sold with Spacelabs 91390 or 91393 monitors.
Look for model number 012-0893-01 on the DVI display cable.
Replace the cable with a model that meets electromagnetic shielding standards.
The cables lack proper shielding, which can cause electromagnetic interference that might disrupt medical devices.
The recall affects DVI display cables used with Spacelabs 91390 and 91393 monitors.
Check for model number 012-0893-01 on the cable, which was sold with specific medical monitors.
We’ve drafted a message you can send Spacelabs Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0169-2026 — Spacelabs Healthcare Spacelabs Healthcare Hello, I own a Spacelabs Healthcare that is covered by recall Z-0169-2026 from Spacelabs Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
