CVE-2020-16239: CWE-287 in Philips SureSigns VS4
When an actor claims to have a given identity, Philips SureSigns VS4, A.07.107 and prior does not prove or insufficiently proves the claim is correct.
AI Analysis
Technical Summary
CVE-2020-16239 is a medium-severity vulnerability identified in Philips SureSigns VS4 medical monitoring devices, specifically versions A.07.107 and prior. The vulnerability is classified under CWE-287, which pertains to improper authentication. In this case, the device does not adequately verify the claimed identity of an actor attempting to access or interact with the system. This insufficient authentication mechanism means that an attacker with some level of access (as indicated by the CVSS vector requiring high privileges) could potentially impersonate a legitimate user or device component. The CVSS 3.1 base score is 4.9, reflecting a medium risk primarily due to the requirement for high privileges (PR:H) and no user interaction (UI:N). The attack vector is network-based (AV:N), meaning the vulnerability can be exploited remotely over a network. The impact is primarily on confidentiality (C:H), with no direct impact on integrity or availability. This suggests that sensitive information handled by the device could be exposed to unauthorized parties if exploited, but the device’s operation and data integrity remain intact. The vulnerability does not have known exploits in the wild, and no patches are currently linked, indicating that mitigation may rely on compensating controls or vendor updates. Given the nature of the device—a vital signs monitor used in clinical settings—unauthorized access could lead to exposure of patient data or manipulation of monitoring data streams, potentially undermining patient privacy and clinical decision-making.
Potential Impact
For European healthcare organizations, this vulnerability poses a significant risk to patient data confidentiality. Philips SureSigns VS4 devices are used in hospitals and clinics to monitor patient vital signs continuously. Exploitation could allow attackers to intercept or access sensitive health information, violating GDPR regulations and potentially leading to legal and reputational consequences. Although the vulnerability does not directly affect device availability or data integrity, unauthorized access to patient data can disrupt clinical workflows and trust in medical devices. Furthermore, healthcare providers in Europe are increasingly targeted by cybercriminals due to the high value of medical data and critical nature of healthcare services. The network-based attack vector increases the risk, especially in environments where medical devices are connected to hospital networks without sufficient segmentation or monitoring. The requirement for high privileges suggests that attackers would need to compromise internal systems or credentials first, but once achieved, the vulnerability could facilitate lateral movement or data exfiltration within healthcare networks.
Mitigation Recommendations
European healthcare organizations should implement strict network segmentation to isolate Philips SureSigns VS4 devices from general IT infrastructure and internet-facing networks. Access controls must be enforced rigorously, ensuring that only authorized personnel with verified credentials can interact with these devices. Multi-factor authentication (MFA) should be applied where possible to increase the difficulty of privilege escalation. Continuous monitoring and logging of device access and network traffic can help detect anomalous behavior indicative of exploitation attempts. Since no official patches are currently available, organizations should engage with Philips for firmware updates or security advisories and apply any recommended fixes promptly. Additionally, conducting regular vulnerability assessments and penetration testing focused on medical device environments will help identify and remediate weaknesses. Training clinical and IT staff on cybersecurity best practices, especially regarding credential management and phishing awareness, will reduce the risk of initial privilege compromise. Finally, organizations should review and update incident response plans to include scenarios involving medical device compromise.
Affected Countries
Germany, France, United Kingdom, Italy, Spain, Netherlands, Belgium, Sweden, Switzerland, Austria
CVE-2020-16239: CWE-287 in Philips SureSigns VS4
Description
When an actor claims to have a given identity, Philips SureSigns VS4, A.07.107 and prior does not prove or insufficiently proves the claim is correct.
AI-Powered Analysis
Technical Analysis
CVE-2020-16239 is a medium-severity vulnerability identified in Philips SureSigns VS4 medical monitoring devices, specifically versions A.07.107 and prior. The vulnerability is classified under CWE-287, which pertains to improper authentication. In this case, the device does not adequately verify the claimed identity of an actor attempting to access or interact with the system. This insufficient authentication mechanism means that an attacker with some level of access (as indicated by the CVSS vector requiring high privileges) could potentially impersonate a legitimate user or device component. The CVSS 3.1 base score is 4.9, reflecting a medium risk primarily due to the requirement for high privileges (PR:H) and no user interaction (UI:N). The attack vector is network-based (AV:N), meaning the vulnerability can be exploited remotely over a network. The impact is primarily on confidentiality (C:H), with no direct impact on integrity or availability. This suggests that sensitive information handled by the device could be exposed to unauthorized parties if exploited, but the device’s operation and data integrity remain intact. The vulnerability does not have known exploits in the wild, and no patches are currently linked, indicating that mitigation may rely on compensating controls or vendor updates. Given the nature of the device—a vital signs monitor used in clinical settings—unauthorized access could lead to exposure of patient data or manipulation of monitoring data streams, potentially undermining patient privacy and clinical decision-making.
Potential Impact
For European healthcare organizations, this vulnerability poses a significant risk to patient data confidentiality. Philips SureSigns VS4 devices are used in hospitals and clinics to monitor patient vital signs continuously. Exploitation could allow attackers to intercept or access sensitive health information, violating GDPR regulations and potentially leading to legal and reputational consequences. Although the vulnerability does not directly affect device availability or data integrity, unauthorized access to patient data can disrupt clinical workflows and trust in medical devices. Furthermore, healthcare providers in Europe are increasingly targeted by cybercriminals due to the high value of medical data and critical nature of healthcare services. The network-based attack vector increases the risk, especially in environments where medical devices are connected to hospital networks without sufficient segmentation or monitoring. The requirement for high privileges suggests that attackers would need to compromise internal systems or credentials first, but once achieved, the vulnerability could facilitate lateral movement or data exfiltration within healthcare networks.
Mitigation Recommendations
European healthcare organizations should implement strict network segmentation to isolate Philips SureSigns VS4 devices from general IT infrastructure and internet-facing networks. Access controls must be enforced rigorously, ensuring that only authorized personnel with verified credentials can interact with these devices. Multi-factor authentication (MFA) should be applied where possible to increase the difficulty of privilege escalation. Continuous monitoring and logging of device access and network traffic can help detect anomalous behavior indicative of exploitation attempts. Since no official patches are currently available, organizations should engage with Philips for firmware updates or security advisories and apply any recommended fixes promptly. Additionally, conducting regular vulnerability assessments and penetration testing focused on medical device environments will help identify and remediate weaknesses. Training clinical and IT staff on cybersecurity best practices, especially regarding credential management and phishing awareness, will reduce the risk of initial privilege compromise. Finally, organizations should review and update incident response plans to include scenarios involving medical device compromise.
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Technical Details
- Data Version
- 5.1
- Assigner Short Name
- icscert
- Date Reserved
- 2020-07-31T00:00:00
- Cvss Version
- 3.1
- State
- PUBLISHED
Threat ID: 6840be00182aa0cae2bfede5
Added to database: 6/4/2025, 9:43:28 PM
Last enriched: 7/7/2025, 1:41:11 AM
Last updated: 8/10/2025, 11:01:28 AM
Views: 15
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