FDAClass IIAugust 12, 2026

GE Healthcare Portrait Core Services SW V 1.2.0 recall: Software Issue

GE Healthcare Portrait Core Services SW V 1.2.0, REF 5700592. patient monitoring system

Why was GE Healthcare Portrait Core Services SW V 1.2.0 recalled?

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).

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

GTIN 00198953056752, Lot/Serial Numbers: SWT25510001TA, 3M1D391215, 3M1D411081, 3M1D411083, 3M1D3B100D, SWT26110010TA, SWT26070001TA, SWT26120008TA, 3M1D411080, 3M1D411082, 3M1D3B100C.

Product
GE Healthcare Portrait Core Services SW V 1.2.0, REF 5700592. patient monitoring system
Recalling firm
GE Medical Systems Information Technologies Inc
Quantity
11 units
Distribution
Worldwide - US Nationwide distribution in the state of MI, and the countries of Czech Republic, Finland, Germany, Netherland, Qatar, UAE.
Recall date
August 12, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls