Cardiac Workstation 5000. Product Number: 860439.
Philips North America Llc · Device will intermittently provide inaccurate data related to native heart rate.
Open FDA's page for this record- Cfres ID
- 221407
- Product res number
- Z-2955-2026
- Event date initiated
- 2026-07-01
- Event date posted
- 2026-08-14
- Recall status
- Open, Classified
- Res event number
- 99361
- Product code
- DPS
- Product description
- Cardiac Workstation 5000. Product Number: 860439.
- Firm FEI number
- 3016618143
- Recalling firm
- Philips North America Llc
- Address 1
- 222 Jacobs St
- City
- Cambridge
- State
- MA
- Postal code
- 02141-2289
- Additional info contact
- Philips Customer Services 800-722-9377
- Reason for recall
- Device will intermittently provide inaccurate data related to native heart rate.
- Root cause description
- Software design
- Product quantity
- 796 units
- Code info
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
- Action
Philips notified consignees on about 07/01/2026 via URGENT Medical Device Correction letter. Consignees were informed that they could continue the use of the device but to refer to the information within the notification letter, disable the automatic Standby feature on the Cardiac Workstation and avoid manually putting the Cardiac Workstation in Standby mode to minimize the inaccurate heart rate value from occurring, and to pass the notice to all those who need to be aware within each organization or to any organization where affected product(s) have been potentially transferred. Additionally, consignees were requested to place the Urgent Medical Device Correction letter with the documentation of the Cardiac Workstation and associated devices in a place where it is most likely to be seen and viewed. Philips representatives will contact consignees to arrange an upgrade to the Cardiac Workstation Release 1.2.0.7.
- Distribution pattern
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.
- K numbers
- K241556
- Harmonized identifiers (openFDA)
- Device name
- Electrocardiograph
- Medical specialty description
- Cardiovascular
- Regulation number
- 870.2340
- Device class
- 2
- K number
- K132758, K082967, K800566, K810154, K241217, K864704, K832421, K870880, K872548, K904606, K922703, K050620, K002074, K844470, K960321, K112959, K811016, K974351, K831429, K221141, K122712, K781054, K881055, K221321, K081473, K142105, K112135, K943709, K790739, K760612, K093211, K851322, K110328, K193415, K142969, K170154, K813022, K822582, K760677, K933065 +536 more
- Registration number
- 3009443693, 3038259592, 1316463, 1523530, 3010536822, 8030978, 1314417, 3010097171, 3011353843, 3001570235, 9617277, 9610105, 3004415095, 3030733800, 3013679558, 3018587883, 3006371704, 3045498928, 3023412068, 3007836437, 1218950, 3003263092, 3003174284, 3013250653, 3021131596, 2000004234, 3031786139, 9611045, 3033959233, 3013596024, 3041276591, 3007029079, 3012027770, 3021559257, 3007384703, 3010082909, 3005521864, 3043226252, 3008921101, 3015142815 +144 more
- FEI number
- 3009443693, 3038259592, 1316463, 1523530, 3010536822, 1314417, 3010097171, 3011353843, 3001570235, 3004415095, 3003190524, 3013679558, 3030733800, 3006371704, 3018587883, 3002807674, 3023412068, 3045498928, 3007836437, 3000957797, 1218950, 3003263092, 3003174284, 3013250653, 3021131596, 2000004234, 3031786139, 3033959233, 3013596024, 3041276591, 3007029079, 3012027770, 3021559257, 3007384703, 3010082909, 3005521864, 3043226252, 3008921101, 3015142815, 3013689228 +144 more
