We are committed to ensuring the safety, effectiveness and security of our products. Cybersecurity of our products and our customer’s infrastructure is an integral part of our focus.
Security researchers play a role in identifying cybersecurity vulnerabilities and concerns. Our goal is to effectively partner with the research community to understand their findings. We are introducing our initial Coordinated Vulnerability Disclosure Process to promote collaboration and reporting of medical device vulnerabilities as described below.
The scope of our vulnerability reporting program includes Medical Devices, Software as a Medical Device, and Mobile Medical Applications. It is not intended to provide technical support information on our products or for reporting Adverse Events or Product Quality Complaints.
To report an adverse event or product quality Complaint, please contact us at stryker.com/productexperience.
If you have identified a potential security vulnerability with one of our Medical Devices, Software as a Medical Device, or Mobile Medical Applications, please submit a vulnerability report to Stryker’s Product Security Team by completing the following form and emailing the completed document to ProductSecurity@stryker.com.
We will not engage in legal action against individuals who submit reports through our Vulnerability Reporting process and enter into a legal agreement with us. We agree to work with individuals who:
What we would like to see from you:
Note: Reports that include only crash dumps or other automated tool output may receive lower priority.
What you can expect from us:
All aspects of this process are subject to change without notice, as well as for case-by-case exceptions. No particular level of response is guaranteed.
In the event, you decide to share any information with Stryker, you agree that the information you submit will be considered as non-proprietary and non-confidential and that Stryker is allowed to use such information in any manner, in whole or in part, without any restriction. Furthermore, you agree that submitting information does not create any rights for you or any obligation for Stryker.
As part of our commitment to product security and customer service, we supply our customers with information to help them assess and address the vulnerabilities and risks.
Specifically, we use the Manufacturer Disclosure Statement for Medical Device Security (MDS²) to provide security information about our products.
The MDS² contains product specific security information related to the capabilities of the devices such as:
The MDS², a universal reporting form which allows us to supply our customers with model-specific information, is endorsed by the American College of Clinical Engineering (ACCE), ECRI (formerly the Emergency Care Research Institute), the National Electrical Manufacturers Association (NEMA), and the Healthcare Information and Management Systems Society (HIMSS).
The form also contains security practice recommendations and explanatory notes from the manufacturer.
SKY CORP 2017-11-47 Rev 1