Spacelabs Healthcare recalls 12-foot DVI display cables (model 012-0895-12) due to electromagnetic interference risks that could interfere with medical devices. Affected units sold with specific lot codes.
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 12-foot DVI display cables that may cause electromagnetic interference with medical devices, potentially compromising patient safety. This recall affects specific model numbers sold with certain lot codes.
The cables lack proper shielding, causing electromagnetic interference that might disrupt the operation of sensitive medical devices. This interference could lead to patient safety risks during medical procedures.
Healthcare facilities using the 91390 or 91393 medical devices with the recalled display cables are most at risk. Patients using these devices could face safety issues if the cables interfere with medical equipment.
Check for model number 012-0895-12 on the cable. Affected units were sold with lot codes (01)10841522131479 (Xprezzon) or (01)10841522131455 (Qube).
Identify the model number on the cable to confirm if it matches 012-0895-12.
Reach out to Spacelabs Healthcare for specific instructions on how to address the issue.
The cables lack proper electromagnetic shielding, which could interfere with medical devices and pose patient safety risks.
Model 012-0895-12 (12-foot DVI-I to DVI-I male/male display cable).
Check for model number 012-0895-12 and lot codes (01)10841522131479 (Xprezzon) or (01)10841522131455 (Qube).
We’ve drafted a message you can send Spacelabs Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0168-2026 — Spacelabs Healthcare Spacelabs Healthcare Hello, I own a Spacelabs Healthcare that is covered by recall Z-0168-2026 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.
