medical MODERATE Updated 2026-09-02

GE Medical Systems Information Technologies Inc recalls PORTRAIT CORE SERVICES SOFTWARE V1.1, Ref# 5700209

See all recalls from GE Medical Systems Information Technologies Inc →

Recalled Product

PORTRAIT CORE SERVICES SOFTWARE V1.1, Ref# 5700209

Share this recall: Facebook X / Twitter WhatsApp Email

Hazard / Issue

Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and will not follow the alarm settings previously configured for each patient or care area.

Issued by

FDA

Affected States: MI, NY
Lot/Code Info: GTIN 00195278679284, Serial Numbers: SWT25250001TA, SWT25360001TA, SWT25360002TA, SWT24090006TA, SWT25100001TA, SWT25120002TA, SWT24140007TA, SWT24150008TA, SWT25100004TA, SWT24050001TA, SWT25110003TA, SWT24180011TA, SWT25120003TA, SWT25230001TA, SWT25230002TA, SWT25110009TA, SWT25110010TA, SWT25230003TA, SWT25230005TA, SWT25230006TA, SWT25230004TA, SWT25260001TA, SWT31240012TA.

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for PORTRAIT CORE SERVICES SOFTWARE →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

Related medical Recalls

SDI Limited recalls Dentsply Sirona Capsule Mixer Model No. 5546068

2026-08-26 · Potential for electrical discharge from unit when unplugged.

Maquet Critical Care AB recalls GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693

2026-08-26 · The module did not undergo electrical safety tests and functional tests during production.

Arrowhead DE LLC recalls Arrow-LOK Implant, REF: 21-253519, 21-253522, 21-253525,

2026-08-26 · Implant did not undergo required gamma radiation dose audit. A potential reduction in sterility assurance could lead to patient infection.

Tobii Dynavox Llc recalls TD Navio Maxi Speech Generating Device Model/Catalog Number

2026-08-26 · Under certain conditions, the battery mounting tabs may become damaged, allowing the battery to move within the device enclosure, potentially leading to an internal short circuit. This may cause localized heating and gas venting within the device enclosure.