FDAFebruary 8, 2019device

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 co...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

draegar medical systemsdraegardraegar medical

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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