Device recalls

Philips Patient Information Center iX REF:866389

Philips North America · Due to software malfunction, patient information system may freeze and become unresponsive.

Open, ClassifiedSoftware designZ-3141-2026
Open FDA's page for this record
Cfres ID
221888
Product res number
Z-3141-2026
Event date initiated
2026-07-31
Event date posted
2026-09-11
Recall status
Open, Classified
Res event number
99566
Product code
MHX
Product description
Philips Patient Information Center iX REF:866389
Code info
All PIC iX software versions 4.0-4.5/UDI: (01)00884838127067
Firm FEI number
3006648320
Recalling firm
Philips North America
Address 1
222 Jacobs St
City
Cambridge
State
MA
Postal code
02141-2296
Additional info contact
Philips Customer Services 800-722-9377
Reason for recall
Due to software malfunction, patient information system may freeze and become unresponsive.
Root cause description
Software design
Product quantity
7359 Units
Action

On July 31, 2026, Philips North America LLC issued an urgent medical device correction to affected consignees via USPS certified mail. Philips requested consignees to take the following actions: Users: 1. In cases where central monitoring has halted, please ensure that triaging of patients at bedside and a change in workflow occurs to more closely monitor patient status. Ensure audible alarm volume is on high in-patient rooms in case bedside devices disconnect and do not provide visual indicators that communication with the central. 2. Pass this notice to those who need to be aware within your organization or to any organization where affected product(s) have been potentially transferred. 3. Place this Urgent notification with the documentation of the Philips Patient Information Center (PIC) iX and associate devices in a place where it is most likely to be seen and viewed. 4. Implement the Technical Solution established by Philips as soon as available within the defined timeframe. Distributors: 1. Send the attached URGENT Medical Device Correction to each customer to whom you have distributed any affected product(s) 2. Perform a good faith effort to reach each customer a minimum of three (3) times, and if possible, using multiple contact methods. 3. Implement the Technical Solution established by Philips as soon as available within the timeframe communicated by Philips, and confirm with Philips the implementation of the correction of all affected product(s). In case any product(s) cannot be corrected, inform Philips of the reason why the Technical Solution could not be implemented.

Distribution pattern

Worldwide - US Nationwide distribution including in the states and territories of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY, PR and the countries of Andorra, Utd. Arab. Emir., Argentina, Austria, Australia, Aruba, Bosnia-Herz., Bangladesh, Belgium, Bulgaria, Bahrain, Bolivia, Brazil, Canada, Switzerland, Chile, Colombia, Costa Rica, Cyprus, Czech Republic, Germany, Denmark, Dominican Rep, Algeria, Estonia, Spain, Finland, Fiji, Faroe Islands, France, United Kingdom, Gibraltar, Guadeloupe, Greece, Hong Kong, Croatia, Hungary, Indonesia, Ireland, Israel, India, Iraq, Iceland, Italy, Jordan, Japan, Kenya, South Korea, Kuwait, Lebanon , Sri Lanka, Lithuania, Luxembourg, Latvia, Libya, Morocco, Monaco, Montenegro, Macedonia, Macao, Martinique, Maldives, Mexico, Malaysia, Namibia, Nicaragua, Netherlands, Norway, New Zealand, Oman, Panama, Peru, Philippines, Pakistan, Poland, Puerto Rico, Portugal, Qatar R¿union, Romania, Serbia, Russian Fed., Saudi Arabia, Sweden, Singapore, Slovenia, Slovakia, Thailand, Turkmenistan, Tunisia, T¿rkiye, Taiwan, Ukraine, Uzbekistan, Vietnam, South Africa.

K numbers
K153702
Harmonized identifiers (openFDA)
Device name
Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Medical specialty description
Cardiovascular
Regulation number
870.1025
Device class
2
K number
K131872, K050141, K131032, K092970, K982279, K062095, K073550, K080157, K090702, K083271, K210906, K062324, K151063, K950264, K151860, K990476, K203435, K101067, K141015, K062194, K070588, K041741, K060541, K983996, K030431, K051400, K073280, K993608, K023475, K172510, K043439, K003248, K203088, K191149, K041790, K221616, K250757, K001433, K040357, K001348 +390 more
Registration number
3009443693, 1316463, 8022257, 3010536822, 3019545235, 3006606827, 3030597679, 8030978, 3012238587, 3011353843, 3001570235, 3009673645, 3012972516, 3021736577, 9610105, 3004415095, 3011120183, 3013679558, 3020115, 3007836437, 3004196561, 1218950, 3003263092, 3007481893, 3013596024, 3021219789, 3010611950, 3021559257, 3005521864, 3003589956, 3004526608, 3030446844, 3003971136, 3008363989, 3008642652, 3010882708, 3007413079, 3022123357, 3007305624, 2032233 +80 more
FEI number
3009443693, 1316463, 3010536822, 3019545235, 3006606827, 3030597679, 3012238587, 3011353843, 3001570235, 3009673645, 3012972516, 3021736577, 3004415095, 3011120183, 3013679558, 3020115, 3007836437, 3004196561, 3000957797, 1218950, 3003263092, 3007481893, 3013596024, 3021219789, 3010611950, 3021559257, 3005521864, 3003589956, 3004526608, 3030446844, 3003971136, 3008363989, 3008642652, 3010882708, 3003757840, 3007413079, 3007305624, 3006147705, 3004977335, 3013501110 +80 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.