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RecallWatchMedical Device Safety
Class IIOngoingZ-2878-2026

GE Medical Systems Information Technologies Inc recalls GE Healthcare Portrait Core Services SW V 1.2.0

GE Medical Systems Information Technologies IncWaukesha, WI, United StatesReported Aug 12, 2026 · 6 days ago
Legal News Analyst ·

Reason for recall

A software vulnerability may allow unauthorized persons to gain privileged access to the device, which could result in loss of patient monitoring, missed patient alarms, and/or access to Protected Health Information (PHI).

Affected product

Check your device

Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.

Affected products & lots

  • GE Healthcare Portrait Core Services SW V 1.2.0, REF 5700592. patient monitoring system
    GTIN 00198953056752
    11 affected lots
    SWT25510001TA3M1D3912153M1D4110813M1D4110833M1D3B100DSWT26110010TASWT26070001TASWT26120008TA
    +3 more3M1D4110803M1D4110823M1D3B100C

What the firm is doing

GE Healthcare issued an URGENT MEDICAL DEVICE CORRECTION to its consignees on 7/10/2026 via traceable means. The notice explained the safety issue, and requested the following: "Actions to be taken by Customer/User You can continue to use Portrait Mobile Monitoring Solution with Portrait Core Services SW V1.2.0, pending GE HealthCare correction. If you need help to identify if your Portrait Mobile Monitoring Solution has Portrait Core Services SW 1.2.0, contact GE HealthCare Service. Ensure that your facility follows all hospital networking and cybersecurity policies and procedures along with the security considerations outlined in the GE HealthCare Portrait Mobile Monitoring Solution Privacy and Security Manual p/n 5970026. Please retain this document for your records." For questions or concerns regarding this notification, please contact GE HealthCare Service at 1-800-437-1171 or a local Service Representative.

DistributionShow details

Worldwide - US Nationwide distribution in the state of MI, and the countries of Czech Republic, Finland, Germany, Netherland, Qatar, UAE.

Class IIWhat this means

Use of the product may cause temporary or medically reversible adverse health consequences.

Sources & references

Taylor Coteus
Legal News Analyst

Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.

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