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MEDICAL DEVICE RECALLMODERATE
Philips Cardiac Workstation 5000
Philips recalls Cardiac Workstation 5000 over intermittent inaccurate heart-rate data.
What to do
Contact Philips North America for instructions on returning or servicing your Cardiac Workstation 5000 to address the intermittent inaccurate heart-rate data.
Why it was recalled
Philips North America is recalling the Cardiac Workstation 5000 (Product Number 860439) because the device may intermittently provide inaccurate data related to native heart rate.
Is mine affected?
Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.
| Product | Recall # | UDI-DI |
|---|---|---|
| Cardiac Workstation 5000. Product Number: 860439. | Z-2955-2026 | 00884838094826 |
| Cardiac Workstation 7000. Product Number: 860441. | Z-2956-2026 | 00884838094833 |
Where it was sold
Distributed nationwide.
Timeline
- Firm initiated recall
- Publicly announced
- Listed on Recall Canary
- Summary updated
Official source
Other Device Defect recalls
Other recent recalls from Philips North America Llc
Editorial summary by Recall Canary · summary updated 2026-08-16 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification