Skip to content
Recall Observatory FDA recall evidence

Device product

Brand Name: Quantum Informatics - VIPER Product Name: Monitor, Physiological, Patient (Without Arrhythmia Detection or Alarms) Product Description: VIPER is a software-only device (SaMD) that is intended to provide near real-time patient safety and clinical best practice solutions for the high-risk patient population in the operating room (OR). VIPER integrates multiple information feeds that supports the real-time distribution of critical patient information and the deployment of advanced active Patient Safety Systems and clinical Best Practice. By integrating compliance, complication, and sophisticated alerting systems, VIPER offers improved support for the avoidance of adverse events.

Z-1695-2025

March 19, 2025

Class II

Product summary

Firm
Spectrum Medical Ltd.
Event
Event 96616
Status
Ongoing
Classification
Class II
Quantity
156 systems
Official record key
device-enforcement:Z-1695-2025

Official wording

Reason: Medical device software marketed without FDA clearance .

Code information: All software revisions/No UDI

Distribution pattern: California, Florida, Illinois, Arkansas, Georgia, Wisconsin, Arizona, Massechusetts, Missouri, Maryland, Colorado, Nebraska, Pennsylvania, New Hampshire, Washington, West Virginia, Texas, Virginia, Minnesota, Distric of Columbia, Ohio, Conneticut, New Jersey, Utah, North Carolina, Louisiana, Kentucky, New York, Kansas, South Carolina, Idaho, Tennessee, Oregon, Maine, Indiana, Oklahoma, New Mexico, North Dakota, Alabama, Michigan, Mississippi

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Medical device software marketed without FDA clearance .