Z-0975-2019 Class II Ongoing
Recall Details
- Product Type
- Devices
- Report Date
- March 13, 2019
- Initiation Date
- February 8, 2019
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 10699 in total
Product Description
Omega Systems These devices are intended to be used in the environment where patient care is provided by Healthcare Professionals, i.e. Physicians, Nurses, and Technicians, who will determine when use of the device is indicated, based upon their professional assessment of the patient's medical condition.
Reason for Recall
The firm is recalling their Delta family of patient monitors software due to cybersecurity vulnerabilities, which may cause the device to reboot, lose functionality, and/or lose communication.
Distribution Pattern
US Nationwide distribution including Puerto Rico.
Code Information
All software versions, all serial numbers.