Precision Ideal Eyes 0502513045Recalls & reported problems
Stryker Corporation · HD Bariatric Laparoscope, Autoclavable, 45 DEG View Direction · Class 2
All models of Precision Ideal Eyes (10)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327059281), received between Dec 29, 2020 and Sep 16, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Fogging” (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
- Fogging2
- No Display/Image1
- Optical Problem1
- Poor Quality Image1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- Insufficient Information1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 16, 2026No Display/Image; Fogging
It was reported that the scope was hooked up at the beginning of the case, both didn't look good. A replacement was obtained and they were able to complete the medical procedure. There may have been a foggy image and/or a full loss of image.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50794462 ↗MalfunctionSep 14, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50765890 ↗MalfunctionDec 29, 2020Poor Quality Image; Optical Problem; Optical Problem
IT WAS REPORTED THAT THERE WAS A BLURRY IMAGE.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 11088011 ↗
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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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