Capsule Technologies SmartLinx Neuron 2 restricted environment protection mechanism failure vulnerability

Summary A restricted environment escape vulnerability exists in the “kiosk mode” function of Capsule Technologies SmartLinx Neuron 2 medical information collection devices running versions 9.0.3 or lower. A specific series of keyboard inputs can escape the restricted environment, resulting in ful...

Multiple Roche Device Permission License and Access Control Vulnerabilities (CNVD-2018-25430)

The Roche Accu-Chek Inform II Instrument, among others, is a handheld blood testing medical device from Roche, Switzerland. A privilege-permission and access-control vulnerability exists in a number of Roche devices, which could be exploited by an attacker to change the configuration...

CVE-2018-8856

Philips e-Alert Unit non-medical device, Version R2.1 and prior. The software contains hard-coded cryptographic key, which it uses for encryption of internal data...

CVE-2018-8854

Philips e-Alert Unit non-medical device, Version R2.1 and prior. The software does not properly restrict the size or amount of resources requested or influenced by an actor, which can be used to consume more resources than intended...

CVE-2018-8852

Philips e-Alert Unit non-medical device, Version R2.1 and prior. When authenticating a user or otherwise establishing a new user session, the software gives an attacker the opportunity to steal authenticated sessions without invalidating any existing session identifier...

CVE-2018-8848

Philips e-Alert Unit non-medical device, Version R2.1 and prior. The software, upon installation, sets incorrect permissions for an object that exposes it to an unintended actor...

CVE-2018-8844

Philips e-Alert Unit non-medical device, Version R2.1 and prior. The web application does not, or cannot, sufficiently verify whether a well-formed, valid, consistent request was intentionally provided by the user who submitted the request...

CVE-2018-8846

Philips e-Alert Unit non-medical device, Version R2.1 and prior. The software does not neutralize or incorrectly neutralizes user-controllable input before it is placed in output that is used as a web page that is then served to other users...

Code injection

Philips e-Alert Unit non-medical device, Version R2.1 and prior. The software, upon installation, sets incorrect permissions for an object that exposes it to an unintended actor...

CVE-2018-8842

Philips e-Alert Unit non-medical device, Version R2.1 and prior. The software transmits sensitive or security-critical data in cleartext in a communication channel that can be sniffed by unauthorized actors. The Philips e-Alert communication channel is not encrypted which could therefore lead to...

Information disclosure

Philips e-Alert Unit non-medical device, Version R2.1 and prior. The Philips e-Alert contains a banner disclosure vulnerability that could allow attackers to obtain extraneous product information, such as OS and software components, via the HTTP response header that is normally not available to t...

CVE-2018-8848

Philips e-Alert Unit non-medical device, Version R2.1 and prior. The software, upon installation, sets incorrect permissions for an object that exposes it to an unintended actor...

CVE-2018-8856

Philips e-Alert Unit non-medical device, Version R2.1 and prior. The software contains hard-coded cryptographic key, which it uses for encryption of internal data...

Cross site request forgery (csrf)

Philips e-Alert Unit non-medical device, Version R2.1 and prior. The web application does not, or cannot, sufficiently verify whether a well-formed, valid, consistent request was intentionally provided by the user who submitted the request...

Session fixation

Philips e-Alert Unit non-medical device, Version R2.1 and prior. When authenticating a user or otherwise establishing a new user session, the software gives an attacker the opportunity to steal authenticated sessions without invalidating any existing session identifier...

CVE-2018-8852

Philips e-Alert Unit non-medical device, Version R2.1 and prior. When authenticating a user or otherwise establishing a new user session, the software gives an attacker the opportunity to steal authenticated sessions without invalidating any existing session identifier...

Code injection

Philips e-Alert Unit non-medical device, Version R2.1 and prior. The software does not properly restrict the size or amount of resources requested or influenced by an actor, which can be used to consume more resources than intended...

Design/Logic Flaw

Philips e-Alert Unit non-medical device, Version R2.1 and prior. The software does not validate input properly, allowing an attacker to craft the input in a form that is not expected by the rest of the application. This would lead to parts of the unit receiving unintended input, which may result ...

CVE-2018-8842

Philips e-Alert Unit non-medical device, Version R2.1 and prior. The software transmits sensitive or security-critical data in cleartext in a communication channel that can be sniffed by unauthorized actors. The Philips e-Alert communication channel is not encrypted which could therefore lead to...

CVE-2018-8844

Philips e-Alert Unit non-medical device, Version R2.1 and prior. The web application does not, or cannot, sufficiently verify whether a well-formed, valid, consistent request was intentionally provided by the user who submitted the request...