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FDA device recallVulnerabilitiesPublished May 14, 2026

Medtronic Neuromodulation: Pump, Infusion, Implanted, Programmable

Updated 2 hours ago ()

Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps should automatically be arranged in consecutive order, from earliest to latest. However, in rare cases, the steps may be displayed out of order. If this occurs, the programmed Flex Infusion schedule will not be delivered at the intended time, if at all.

Tags
FDA recall, medical device, class 3, Unknown, Under Investigation by firm, Open, Classified
Related exam domains
CISSP 3: Security Architecture and Engineering; CISSP 8: Software Development Security
Source record id
Z-2201-2026
First seen by InfoSec Signals
Sep 23, 2026

Source: openFDA device recalls, U.S. Food and Drug Administration about this source more from it

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.

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