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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/Diagnostic Equipment

GE Medical Systems, SCS: Firm has identified a security vulnerability in AW Server products. If exploited, a malicious actor could compromise the confidentiality, integrity, and availability of patient data.

Agency Publication Date: October 8, 2025
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Summary

GE Medical Systems has recalled AW Server versions 2.0, 3.0, 3.1, and 3.2 due to a critical security vulnerability. This software is used in medical imaging systems to process and manage patient data. The defect involves a cybersecurity weakness that could allow unauthorized access to sensitive medical information.

Risk

A malicious actor could exploit this vulnerability to compromise the confidentiality, integrity, and availability of patient medical data. If patient records are altered or made unavailable, it could lead to incorrect diagnoses or delays in medical treatment.

What You Should Do

  1. Identify if your facility uses AW Server versions 2.0, 3.0, 3.1, or 3.2 by checking the System ID or UDI-DI 00840682102384.
  2. Check your specific System ID against the affected list (e.g., 907729AWS1, 720238AW1, 205934AWSRV) provided in the product documentation.
  3. Contact GE Medical Systems, SCS immediately to receive specific security patches or instructions to mitigate the identified vulnerability.
  4. Ensure your internal IT and cybersecurity teams are alerted to monitor for any unauthorized access or unusual activity on the AW Server network.
  5. Call the FDA medical device hotline at 1-888-463-6332 if you have additional questions regarding this safety alert.

Affected Products

Product: AW Server 2.0
Model / REF:
907729AWS1
720238AW1
907ULMCCT
205934AWSRV
205975AWSRV
205971AWS
205510VAW
205815AWS2
UABMAWS1
749153GE3
UABMRPET
256593AW1
256265AWS4
256265AWS3
205481AWS1
251343AWS
251665MCIAWS
251316VAWS
251435AW5
251435AWSMARTSUB1
303584HP
251435AWSSMARTSUB1
256386AW1
205RCAWS
870423AWSMARTSUB1
870642AWS
718329SMART11
479314AWS1
479314AWS2
870207AW1
501686AWS31
501978AW1
501686AWSMARTSUB2
501552AW2
501202AWS1
501686AWSMARTSUB1
479338AWS
928773AWS
928214AWS
480256AWS
928757AWEN
Product: AW Server 3.0
Model / REF:
UDI-DI 00840682102384
Product: AW Server 3.1
Model / REF:
UDI-DI 00840682102384
Product: AW Server 3.2
Model / REF:
UDI-DI 00840682102384

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97657
Status: Active
Manufacturer: GE Medical Systems, SCS
Manufactured In: France
Units Affected: 7,302 (1,381 US; 5,921 OUS)

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.

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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.