SwitchPoint Infinity, iSuite 0678003000Recalls & reported problems
Stryker Communications Inc. · Infinity 3, Lite Video Router · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327054255), received between Mar 13, 2024 and Mar 13, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “No Display/Image” (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.
Reports received per month
Most reported problems
Device problems
- No Display/Image1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 13, 2024No Display/Image; No Display/Image
IT WAS REPORTED THAT THE ENDO CAM IMAGE WOULD NOT DISPLAY AFTER PATIENT HAD BEEN PLACED UNDER ANESTHESIA. ENDO CAM FAULT HAPPENED PRIOR TO SURGERY AND COULD NOT BE RESOLVED. PATIENT HAD TO BE WOKE UP FROM ANESTHESIA AND SURGERY RE-SCHEDULED. THERE WERE NO REPORTED INJURIES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18898311 ↗
Other Endoscopic video imaging system/component, gastroenterology-urology devices
- SwitchPoint Infinity, iSuite 0678001000Stryker 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.