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FDA device recallVulnerabilitiesPublished Jun 3, 2026
Fresenius Kabi USA, LLC: Pump, Infusion
Updated 2 hours ago ()
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.
- 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
- Sep 23, 2026
Source: openFDA device recalls, U.S. Food and Drug Administration about this source more from it
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