SwitchPoint Infinity, iSuite 0678001000Recalls & reported problems
Stryker Communications Inc. · Infinity 3, Video Router · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327054156), received between Sep 7, 2023 and Sep 7, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Erratic or Intermittent Display” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Erratic or Intermittent Display1
Patient problems
- Bowel Perforation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 7, 2023Erratic or Intermittent Display; Erratic or Intermittent Display
IT WAS REPORTED THAT WHEN ALL THE MONITORS WERE FLICKERING, THE SURGEON PUNCTURED THE PATIENT'S BOWEL WHILE INSERTING A TROCAR AND HAD TO CONVERT TO OPEN PROCEDURE. AN ADDITIONAL MEDICAL INTERVENTION WAS PERFORMED DUE TO THE PUNCTURED BOWEL.
Patient problems: Bowel Perforation
MAUDE report 17703359 ↗
Other Endoscopic video imaging system/component, gastroenterology-urology devices
- SwitchPoint Infinity, iSuite 0678003000Stryker Communications Inc. · Endoscopic video imaging system/component, gastroenterology-urology1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.