Reported Aug 26, 2026 · Ongoing · Updated Sep 16, 2026

Cardiac Workstation 7000. Product Number: 860441.

Philips North America LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Philips North America Llc · 222 Jacobs St · Cambridge, MA · 02141-2289

Is this the product you have?

  • Cardiac Workstation 7000
  • Product Number860441
Lot codes and dates
  • Product Number860441
  • UDI(01)00884838094833
  • Serial Numbers

    348 of 348 codes

    • US22520232
    • US32520244
    • US32520248
    • US42520323
    • US42520320
    • US42520300
    • US52520333
    • US52520332
    • US52520345
    • US52520382
    • US52520359
    • US52520390
    • US52520373
    • US52520412
    • US52520420
    • US52520426
    • US52520461
    • US62520469
    • US62520470
    • US62520474
    • US62520476
    • US62520483
    • US72520504
    • US72520518
    • US72520531
    • US62520499
    • US72520500
    • US72520648
    • US72520526
    • US72520524
    • US72520522
    • US72520517
    • US72520590
    • US72520547
    • US72520592
    • US82520720
    • US72520603
    • US72520640
    • US72520580
    • US72520666
    • US82520755
    • US82520752
    • US82520762
    • US72520662
    • US72520652
    • US72520664
    • US82520771
    • US82520844
    • US82520782
    • US82520774
    • US82520769
    • US82520777
    • US82520775
    • US82520855
    • US82520820
    • US82520823
    • US82520824
    • US82520744
    • US72520678
    • US82520822
Amount recalled
1,810 units

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

Device will intermittently provide inaccurate data related to native heart rate.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Philips North America LLC recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (Enforcement Report)

Read the FDA (weekly enforcement report) notice

Data as of Sep 19, 4:17 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.