VisionPro, SYNK 0240031000Recalls & reported problems
Stryker Corporation · 26 Inch Wireless LED Display · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 07613327056068), received between Jul 10, 2018 and May 22, 2024 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Device Fell” (2 reports).
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
- Device Fell2
- Output Problem2
- Mechanical Problem1
- No Display/Image1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 22, 2024Device Fell; Device Fell
IT WAS REPORTED THAT THE MONITOR FELL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19378165 ↗MalfunctionMay 22, 2024Device Fell; Device Fell
IT WAS REPORTED THAT THE MONITOR FELL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19378163 ↗MalfunctionNov 17, 2023Output Problem; Output Problem
IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18166294 ↗MalfunctionJun 15, 2022Output Problem; No Display/Image; Output Problem
IT WAS REPORTED THE DEVICE LOST IMAGE FOR 2-3 MINUTES DURING A PROCEDURE. THERE WERE NO ADVERSE CONSEQUENCES AS A RESULT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14702552 ↗MalfunctionJul 10, 2018Mechanical Problem
IT WAS REPORTED THAT THE MONITOR FELL. THE NURSE NEEDED NO TREATMENT AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7674290 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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