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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices

GE Healthcare: Centricity Diagnostic Viewers Recalled for Cybersecurity Vulnerability

Agency Publication Date: March 28, 2025
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Summary

GE Healthcare is recalling several diagnostic imaging software systems, including Centricity Universal Viewer, PACS-IW, Radiology RA600, and Cardiology CA1000, affecting approximately 4,935 units worldwide. These systems have a potential security vulnerability where service login passwords can be identified, which could allow a hacker to gain unauthorized access to the software. If accessed, a malicious actor could potentially change, delete, or manipulate sensitive patient data. Consumers should contact their healthcare provider or GE Healthcare directly for guidance on securing their systems.

Risk

The flaw involves identifiable service login credentials that could permit unauthorized access to medical imaging databases. This poses a significant risk to patient safety and privacy as it could lead to the unauthorized manipulation of clinical records or diagnostic results.

What You Should Do

  1. Check your diagnostic imaging system to identify if you are using GE Healthcare Centricity Universal Viewer (UV), Centricity PACS-IW, Centricity Radiology RA600, or Centricity Cardiology CA1000.
  2. Verify the software model numbers and System IDs against the extensive list of affected hardware, including model numbers such as 2066908-077, 2033901-001, 2038437-001, 2049587-015, and 2109571-002.
  3. Identify your specific Installed Product ID or System ID, which can be found in the system settings or facility inventory records, and cross-reference it with the recall data to confirm if your installation is vulnerable.
  4. Contact your facility's IT and cybersecurity departments to monitor for any unauthorized access attempts on diagnostic viewing platforms.
  5. Contact GE Healthcare technical support immediately to receive specific security guidance and instructions on required software patches or security configuration updates.
  6. Healthcare professionals should consult with the manufacturer for further technical instructions or to discuss potential system remedies.
  7. For additional information, contact the FDA at 1-888-463-6332 or visit the medical device recall section at www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

📋Other Action

Technical Security Advisory and guidance

How to: Contact your healthcare provider or the manufacturer for further instructions regarding system security configuration or potential software patches.

Affected Products

Product: GE Healthcare Centricity Universal Viewer (UV)
Model / REF (72):
2066908-077
2066908-136
2066908-150
2088026-003
2088026-026
2088026-032
2088026-043
2088026-110
2088026-115
2088026-132
2088026-306
2088026-308
2088026-406
2088026-506
2088026-614
2088026-713
2088026-714
2088026-715
2088026-723
2088026-806
2088026-906
2088026-936
2088026-940
2088026-943
2088026-946
2088026-948
2088026-957
2088026-959
2088026-960
2088026-961
2088026-962
2088026-967
2088026-969
2088026-970
2088026-971
2088026-973
2088026-985
2088026-989
2088026-990
2088026-993
2088026-994
2089629-003
2100169-001
2100491-006
2100491-012
2102675-010
2102675-101
2102676-001
2104867-001
2104867-044
Lot Numbers:
HCIT1584981UV
RSMKG-SERPONG02
KE2701UV01
KE0301UV01
M4172630
DZ1128PP02
KE1111UV01
PACS-IW-479
HCIT1543321UV
ZA1352PP02
ADVENTIST01970561
0853550218
QUEEN19630915
Product: GE Healthcare Centricity PACS-IW (PACS-IW)
Model / REF:
2042988-001
2049587-009
2049587-011
2049587-012
2049587-015
2049588-012
2052829-001
Lot Numbers:
HCIT4250187IW
PACS-IW-168
PACS-IW-477
PACS-IW-412
AZ4030PC01
RU1016ID01
RU2967RW01
PACS-IW-17
DRMC00558370
PACS-IW-340
Product: GE Healthcare Centricity Radiology RA600 (RA600)
Model / REF:
2022296-001
2033901-001
2038437-001
2038437-011
2038437-012
2038437-013
2038437-014
2038437-0XX
2098071-004
2109571-002
2109571-006
2109571-010
2109594-009
2109594-011
K2090PS
K2090PTED
MANLEGACY114
MANLEGACY64
Lot Numbers:
NDMGRA01
AH5045RW01
AP0701RW01
520784RA6CLSW3
928729RA600SW2
818901RA600SW1
NOIRA010
CARTI22218186
FAWCETTME23230047
AL4023RW01
Product: GE Healthcare Centricity Cardiology CA1000 (CA1000)
Model / REF:
2033901-001
2038437-001
2038437-009
2038437-014
2038437-015
2038437-0XX
2109571-007
2109571-010
2109571-011
2109571-012
MANLEGACY111
MANLEGACY112
MANLEGACY47
P00011TS
Lot Numbers:
HCIT4082079CA1000
520855CA1SW1
SVMCA6
BIHT22144957
CAMC01893386
DR_SRUJAL_SHAH_CA1000_20
397713PC01
Product: GE Healthcare Centricity Centricity PACS-IW with Universal Viewer
Model / REF:
2049587-015
2066908-086
2066908-136
2104867-045
Lot Numbers:
PACS-IW-126
GA001PACTRL01
ZA2533PAC1
HC3062UV01

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96375
Status: Active
Manufacturer: GE Healthcare
Sold By: Authorized GE Healthcare dealers; Specialty medical software retailers
Manufactured In: United States
Units Affected: 5 products (2653 units; 82 units; 1563 units; 633 units; 4 units)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.