Philips recalls Cardiac Workstation 7000 model 860441 due to power short risk from a pinched wire. Affected units may cause electrical issues.
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 Cardiac Workstation 7000 devices with model number 860441 because a pinched power wire can cause a short. This could lead to electrical issues if the device is used.
A pinched power module wire inside the device housing can cause a short circuit. This short may lead to electrical issues but does not typically cause serious injury in normal use.
Healthcare professionals using the Cardiac Workstation 7000 in medical settings are most at risk. The recall affects specific model numbers sold in the U.S.
Check for model number 860441 on the device. Affected units have serial numbers starting with US followed by numbers like 42520284.
Look for model number 860441 on the device label.
The recall is for a potential power short risk, but it does not typically cause serious injury in normal use.
Check for model number 860441 and serial numbers starting with US followed by numbers like 42520284.
The recall does not specify a remedy, so no action is required beyond checking if your device is affected.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0166-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-0166-2026 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.
