Spacelabs Healthcare recalls 6-foot DVI display cables (model 012-0895-01) due to inadequate shielding causing electromagnetic interference that may disrupt medical devices. 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 due to poor shielding. This poses a serious risk to patient safety during medical procedures.
The display cables lack proper electromagnetic shielding, which can cause interference with other medical devices. This interference may disrupt critical medical equipment during patient care, potentially causing serious harm.
Healthcare facilities using the 91390 or 91393 monitors with these display cables are affected. Patients undergoing medical procedures with improperly shielded cables are at highest risk.
Check for the model number 012-0895-01 on the cable. These cables were sold with Spacelabs 91390 and 91393 monitors. Lot codes include (01)10841522131479 (Xprezzon) and (01)10841522131455 (Qube).
Discontinue use of the recalled DVI display cables (model 012-0895-01) as they pose a serious risk to patient safety.
The cables lack proper electromagnetic shielding, which can interfere with medical devices during patient care, posing a serious risk to patient safety.
Look for model number 012-0895-01 on the DVI display cable.
These cables were used with Spacelabs 91390 and 91393 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-0167-2026 — Spacelabs Healthcare Spacelabs Healthcare Hello, I own a Spacelabs Healthcare that is covered by recall Z-0167-2026 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.
