Lower risk Medical device recall · FDA · Published July 1, 2026

Philips Cardiac Workstation 5000: Inaccurate Heart Rate Data Risk

Philips recalls Cardiac Workstation 5000 (product number 860439) due to potential inaccurate native heart rate data. Affected units include specific serial numbers listed in the recall.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2955-2026Medical device Philips ›

Lower-risk recall

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

✎ GovInfoNow plain-language explainer

Philips is recalling its Cardiac Workstation 5000 devices because they may provide inaccurate heart rate readings. This could lead to incorrect medical decisions if the device is used for heart monitoring. Read more at govinfonow.com/recall/697947-philips-cardiac-workstation-5000-inaccurate-heart-rate-data-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/697947-philips-cardiac-workstation-5000-inaccurate-heart-rate-data-risk · Updated September 14, 2026 · FDA enforcement record: FDA #Z-2955-2026

Cite this page

“Philips Cardiac Workstation 5000: Inaccurate Heart Rate Data Risk.” GovInfoNow, updated September 14, 2026. https://govinfonow.com/recall/697947-philips-cardiac-workstation-5000-inaccurate-heart-rate-data-risk. Based on FDA recall #Z-2955-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2955-2026%22&limit=1).

Philips North America LLC is recalling Cardiac Workstation 5000 units due to a hazard where the device may intermittently provide inaccurate heart rate data, according to the FDA. The recall was announced on July 1, 2026.

How to tell if you have it

Brand: Philips
Product: Cardiac Workstation 5000
Product Number: 860439
UPC: 00884838094826
Units affected: 796

The hazard

The Cardiac Workstation 5000 device will intermittently provide inaccurate data related to native heart rate, according to the FDA.

Context

GovInfoNow's records show Philips North America LLC has issued 129 other recalls since July 12, 2017. Recent Philips recalls include Ingenia 3.0T and Ingenia 3.0T CX units on Aug. 21, 2026, and Spectral CT 7500 software on Aug. 18, 2026. Other recent recalls of similar products include Boston Scientific LUX-Dx II Plus Model M312 (March 30, 2026) and Boston Scientific CRT-P Pacemakers (March 19, 2026).

How to tell if you have this one

Check for the product number 860439 and specific serial numbers listed in the recall notice. The device is sold under Philips North America LLC.

Brand
Philips
Product
Cardiac Workstation 5000. Product Number: 860439
Category
Medical device

FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class II
Status
Ongoing
Distribution
Worldwide distribution - US Nationwide and the countries of Australia, Austria, Bahrain, Belgium, Brazil, Canada, Croatia, Czech Republic, Dominican Republic, France, Germany, Gibraltar, Hong Kong, Iceland, Ireland, Iraq, Italy, Luxembourg, Malta, Netherlands, New Caledonia, New Zealand, Norway, Poland, Portugal, Qatar, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, United Arab Emirates, United Kingdom.

Recall number	Product, codes & lots	Quantity
Z-2955-2026	Cardiac Workstation 5000. Product Number: 860439.; Product Number: 860439. UDI: (01)00884838094826. Serial Numbers: US42510185, US42510184, US52510209, US52510200, US52510226, US52510228, US62510247, US62510250, US62510256, US72510286, US82510299, US82510307, US82510300, US82510313, US82510318, US82510314, US82510335, US82510336, US82510341, US82510325, US92510351, US92510353, US92510354, US92510361, US92510362, US92510370, USN2510413, USN2510414, USN2510434, USN2510435, USN2510437, USD2510506, USD2510519, US12610582, USD2510513, US12610598, US22610609, US22610683, US22610691, US22610689, US32610737, US32610744, US32610759, US32610766, US32610749, US32610739, US32610751, USD2510516, USD2510510, USD2510517, USD2510529, USD2510509, US32610752, US32610753, US32610879, US32610880, US32610901, US32610914, US42610946, US32610915, US32610941, US32610932, US42610943, US42610942, US42610959, US42610958, US42610955, US42610974, US42610967, US42610956, US42610993, US42610960, CN72410032, CN92410061, CNO2410064, CNO2410068, CNN2410075, CND2410080, CND2410101, CND2410103, CN12510116, CN12510136, CN22510140, CN22510142, CN22510146, CN32510148, CN32510161, CN42510168, CN42510181, CN42510183, CN52510204, CN52510201, CN52510217, CN62510239, CN62510241, CN62510242, CN62510253, CN62510254, CN62510251, CN72510275, CN72510282, CN72510281, CN72510285, CN72510289, CN72510288, CN72510293, CN72510297, CN82510305, CN82510310, CN82510323, CN82510324, CN82510321, CN92510343, CN92510364, CN92510365, CN92510367, CN92510374, CNO2510380, CNO2510392, CNO2510383, CNO2510386, CNO2510396, CNN2510412, CNN2510410, CNN2510427, CNN2510443, CNN2510444, CNN2510454, CNN2510485, CNN2510486, CND2510503, CND2510502, CND2510508, CND2510528, CND2510530, CND2510566, CND2510575, CND2510574, CN12610585, CN12610590, CN12610595, CN12610593, CN22610612, CN22610681, CN22610707, CN22610735, CN32610755, CN32610760, CN32610761, CN32610762, CN32610763, CN32610765, CN32610818, CN32610826, CN32610910, CN32610913, CN32610912, CN32610924, CN32610923, CN32610929, CN32610930, CN32610933, CN42610944, CN42610951, CN42610970, US42610994	796 units
Z-2956-2026	Cardiac Workstation 7000. Product Number: 860441.; Product Number: 860441. UDI: (01)00884838094833. Serial Numbers: 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, US82520821, US82520726, US72520667, US72520670, US72520668, US82520848, US72520669, US92520885, US82520857, US82520851, US82520863, US92520881, US92520890, US92520901, US92520903, US92520894, US92520905, US92520906, US92520981, USO2521043, USO2521042, USO2521050, USO2521128, USO2521092, USO2521122, USO2521065, USN2521141, US92520990, USN2521132, USN2521144, USN2521149, USN2521130, USN2521179, USN2521150, USN2521161, USN2521163, USN2521164, USN2521160, USO2521072, USN2521175, USN2521170, USN2521176, USN2521185, USN2521206, USN2521211, USN2521214, USN2521213, USN2521196, USN2521226, USN2521223, USN2521249, USN2521215, USN2521224, USN2521246, USN2521243, USN2521235, USN2521221, USN2521222, USN2521342, USN2521198, USN2521254, USN2521252, USN2521294, USN2521286, USN2521258, USN2521257, USN2521256, USN2521307, USN2521288, USN2521287, USD2521394, USN2521289, USN2521300, USN2521296, USD2521365, USN2521302, USD2521427, USD2521407, USD2521436, USD2521433, USD2521448, USD2521440, USD2521475, USD2521430, USN2521308, USD2521362, USD2521374, USN2521309, USD2521355, US12621548, US12621550, US12621553, US12621671, US12621672, US12621629, US12621713, US12621712, US12621711, US12621710, US22621762, US22621763, US22621777, US22621787, US22621796, US22621859, US32621881, US32621887, US32621893, US32621905, US32621886, US32621884, US32621894, US32621906, US32621907, US32621909, US32621910, USD2521420, USD2521409, USD2521411, USD2521416, USD2521422, US32621911, US32621918, US32621912, US32621913, US32621936, US32622017, US32621923, US32621980, US32621953, US32621952, US32621950, US32621954, US32621895, US32622011, US32622018, US32622051, US32622023, US32622077, US32622078, US32622046, US42622153, US32622027, US32622053, US32622052, US32622076, US32622064, US42622108, US32622065, US42622129, US42622123, US42622110, US42622148, US42622113, US42622111, US42622154, US42622147, US42622139, US42622146, US42622116, US42622149, US42622150, US42622222, US42622188, US42622183, US42622187, US42622156, US42622184, CN72420050, CN82420071, CNO2420085, CNN2420093, CNN2420096, CNN2420111, CNN2420115, CND2420119, CND2420145, CND2420134, CND2420150, CND2420151, CND2420168, CND2420167, CND2420169, CND2420171, CN12520174, CN22520206, CN22520215, CN22520218, CN22520214, CN22520226, CN22520242, CN32520246, CN42520274, CN42520317, CN42520291, CN52520389, CN52520379, CN52520445, CN52520460, CN52520454, CN62520466, CN62520487, CN72520565, CN72520650, CN72520631, CN82520721, CN72520651, CN82520758, CN82520764, CN82520791, CN82520792, CN82520793, CN82520837, CN82520842, CN82520864, CN82520809, CN92520880, CN92520871, CN92520923, CN92520929, CN92520970, CN92520935, CN92520979, CN92520976, CNO2521015, CNO2520997, CNO2521008, CNO2521007, CNO2521026, CNO2521030, CNO2520998, CNN2521156, CNN2521212, USN2521219, CNN2521230, CNN2521283, CNN2521260, USN2521291, CNN2521346, CNN2521345, CNN2521344, CNN2521343, CND2521375, CND2521352, CND2521415, CND2521439, USD2521429, CND2521506, CN12621557, CND2521535, CND2521544, CN12621562, CN12621580, CN12621577, CN12621576, CN12621579, CN12621690, CN12621687, CN12621696, CN12621697, CN12621698, CN22621734, CN22621799, CN22621798, CN32621877, CN22621874, CN32621875, CN32621888, CN32621890, CN32621896, CN32621968, CN32621997, CN32622002, CN32621990, CN32621983, CN32622007, CN32622008, CN32622005, CN32622006, CN32622021, CN32622047, CN32622066, CN32622075, CN42622107, CN42622124, CN42622134, CN42622220, CN42622221	1,810 units

Based on the official FDA remedy

What to do — step by step

Check Device Serial Number
Look for the serial number on the device label or documentation to confirm if it's affected.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

FDA distribution: “Worldwide distribution - US Nationwide and the countries of Australia, Austria, Bahrain, Belgium, Brazil, Canada, Croatia, Czech Republic, Dominican Republic, France, Germany, Gibraltar, Hong Kong, Iceland, Ireland, Iraq, Italy,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 56 days after the firm started it.

Jul 1, 2026Firm started the recall
Aug 14, 2026FDA classified it Class II
Aug 26, 2026Published in FDA’s Enforcement Report
Sep 8, 2026Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

How can I tell if my device is affected?

Check the serial number against the list provided in the recall notice. Affected units have specific serial numbers starting with US42510185, US42510184, and others listed in the record.

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Keep exploring

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Link to this recall

<a href="https://govinfonow.com/recall/697947-philips-cardiac-workstation-5000-inaccurate-heart-rate-data-risk">Philips Cardiac Workstation 5000: Inaccurate Heart Rate Data Risk (GovInfoNow)</a>

Where this comes from

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.

Official source: FDA Recall #Z-2955-2026 (July 1, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2955-2026 to see it in context.
Plain-language summary written by qwen3:4b on September 14, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.