Z-0975-2019 Class II Ongoing

Recalled by Draegar Medical Systems, Inc. — Andover, MA

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.