FDA recall Z-0975-2019

Draegar Medical Systems, Inc. · Class II · device

Product

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

US Nationwide distribution including Puerto Rico.

Key facts

Status
Ongoing
Initiation date
2019-02-08
Report date
2019-03-13
Voluntary/Mandated
Voluntary: Firm initiated
Location
Andover, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0975-2019