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FDA (Device enforcement)Recalled 2026-07-31class ii

Philips North America: Philips Patient Information Center iX REF:866389

Is my product affected?

Philips Patient Information Center iX REF:866389

  • UPC 00884838127067

Check against the official notice below — it lists the full affected range.

Hazard

Due to software malfunction, patient information system may freeze and become unresponsive.

Details from the source

Reason for recall: Due to software malfunction, patient information system may freeze and become unresponsive. Distribution: 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, Quantity: 7359 Units Lot/code info: All PIC iX software versions 4.0-4.5/UDI: (01)00884838127067

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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