1188 1188210105Recalls & reported problems
Stryker Corporation · HD Camera Head, C-Mount, with 3 m Cable · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327063332), received between Jul 12, 2019 and Aug 27, 2025 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Poor Quality Image” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Poor Quality Image2
- Insufficient Device Problem Information1
- Output Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Code Available1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 27, 2025Poor Quality Image; Output Problem; Poor Quality Image; Output Problem
IT WAS REPORTED THAT THERE WAS BRIGHT IMAGES. THEREFORE, THERE WAS OVEREXPOSED IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22905650 ↗MalfunctionSep 17, 2019Poor Quality Image
IT WAS REPORTED THAT THE IMAGE WAS DARK. THE PROCEDURE WAS COMPLETED SUCCESSFULLY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9077839 ↗InjuryJul 12, 2019Insufficient Device Problem Information
IT WAS REPORTED THAT THE PROCEDURE WAS CONVERTED TO AN OPEN PROCEDURE.
Patient problems: No Code Available
MAUDE report 8786207 ↗
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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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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