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FDA device recallVulnerabilitiesPublished June 3, 2026
Fresenius Kabi USA, LLC: Pump, Infusion
Potential software anomaly that can cause the pump to report a false battery-health value (typically 69%) and trigger a battery-depletion alarm that will shut down the pump unless it is reconnected to AC mains power.
Open the source record- Tags
- FDA recall, medical device, class 2, General Hospital, Software design (manufacturing process), Open, Classified
- Related exam domains
- CISSP 3: Security Architecture and Engineering; CISSP 8: Software Development Security
- Source record id
- Z-2223-2026
- First seen by InfoSec Signals
- 9/23/2026
Exam domain labels come from a keyword heuristic and are study hints, not an official mapping. The summary is the publisher's own text, shortened; the linked record is authoritative.