Philips recalls Cardiac Workstation 5000 model 860439 due to power module wire failure causing short circuits. Affected units may have short circuits that could lead to equipment malfunction.
Failure of Environmental Stress Testing from a pinched power module wire within the housing of the Cardiac Workstation device which resulted in a short.
Philips is recalling its Cardiac Workstation 5000 model 860439 because a power module wire can fail under stress, causing short circuits. This could lead to equipment malfunction, though serious injury risks are not specified in the recall.
A pinched power module wire inside the device can fail under environmental stress, causing a short circuit. This short circuit may lead to equipment malfunction but does not specify a risk of serious injury.
Healthcare professionals using the Cardiac Workstation 5000 model 860439 are likely affected. Those in medical settings with this equipment are at the highest risk.
Check for the model number 860439 on the Cardiac Workstation 5000 device. The recall includes units sold with this specific model number.
Look for the model number 860439 on the Cardiac Workstation 5000 device.
The recall does not specify a risk of serious injury.
Check for the model number 860439 on the device.
The recall does not provide specific action steps beyond checking the model number.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0165-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-0165-2026 from Philips. 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.
