Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Omega Systems These devices are intended to be used in Recalled by Draegar Medical Systems, Inc. Due to The firm is recalling their Delta family of...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Draegar Medical Systems, Inc. directly.
Affected Products
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.
Quantity: 10699 in total
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Draegar Medical Systems, Inc.
Draegar Medical Systems, Inc. has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report