Precision Ideal Eyes 0502503010Recalls & reported problems
Stryker Corporation · HD Laparoscope, Autoclavable, 0 DEG View Direction · Class 2
All models of Precision Ideal Eyes (10)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This Stryker Precision Ideal Eyes laparoscope is a reusable, autoclavable HD surgical scope. Most of its 72 adverse event reports describe image problems — blurry or poor quality pictures, fogging during a procedure, or a scope breaking — and 2 reports involved an injury. There were no deaths. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 74
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 74 adverse event reports that list this exact device (DI 07613327059151), received between Apr 24, 2019 and Sep 9, 2026 — classified as 2 injuries, 72 malfunctions.
The most frequently reported specific device problem is “Poor Quality Image” (50 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 Image50
- Optical Problem33
- Break8
- Fogging7
- No Display/Image6
- Optical Distortion3
- Crack2
- Moisture Damage2
Patient problems
- No Clinical Signs, Symptoms or Conditions64
- Insufficient Information35
- No Known Impact Or Consequence To Patient11
- Burn, Thermal1
- No Consequences Or Impact To Patient1
- Unspecified Gastrointestinal Problem1
Recent adverse event reports
The 25 most recent of 74 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 9, 2026Fogging
It was reported that the scope had dark and cloudy image and the moisture in the scope cannot be wiped off.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50695892 ↗MalfunctionSep 1, 2026No Display/Image
It was reported that the lens is blurry and it cant be seen out of.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50534329 ↗MalfunctionAug 31, 2026No Display/Image
It was reported that the lens is blurry and it cant be seen out of.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50534269 ↗MalfunctionAug 31, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50531283 ↗MalfunctionAug 26, 2026No Display/Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50463768 ↗MalfunctionAug 14, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50259967 ↗MalfunctionAug 11, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50216054 ↗MalfunctionFeb 23, 2026Fogging
IT WAS REPORTED THAT FOG HAS FORMED ON THE SCOPE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24422471 ↗MalfunctionOct 30, 2024Fogging; Moisture or Humidity Problem; Fogging; Moisture or Humidity Problem
IT WAS REPORTED THAT THERE WAS FOGGY IMAGE DURING THE PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20570932 ↗MalfunctionApr 17, 2024Fogging; Fogging
IT WAS REPORTED THAT THERE WAS FOGGY IMAGE DURING THE PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19129489 ↗MalfunctionDec 22, 2023No Display/Image; Poor Quality Image; No Display/Image; Poor Quality Image
IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE DURING PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18384482 ↗MalfunctionDec 20, 2023Poor Quality Image; Optical Problem; Poor Quality Image; Optical Problem
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE DURING PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18366457 ↗MalfunctionNov 16, 2023Poor Quality Image; Poor Quality Image
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18154700 ↗MalfunctionOct 12, 2023Poor Quality Image; Poor Quality Image
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17926793 ↗MalfunctionSep 6, 2023Poor Quality Image; Poor Quality Image
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17693106 ↗MalfunctionAug 9, 2023Poor Quality Image; Poor Quality Image
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17493735 ↗MalfunctionAug 2, 2023Output Problem; Output Problem
IT WAS REPORTED THAT THE SCREEN BECAME BLACK. THE PATIENT'S GALLBLADDER WAS INJURED AND IT RESULTED IN ITS REMOVAL. THE ORIGINAL PLANNED PROCEDURE WAS NOT PERFORMED AND WAS CANCELLED.
Patient problems: Unspecified Gastrointestinal Problem
MAUDE report 17447121 ↗MalfunctionJul 5, 2023Optical Problem; Optical Problem
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17261992 ↗MalfunctionJun 16, 2023Optical Problem; Optical Problem
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17148445 ↗MalfunctionMay 25, 2023Optical Problem; Optical Problem
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17007595 ↗MalfunctionMay 25, 2023Optical Problem; Optical Problem
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17004867 ↗MalfunctionMay 22, 2023Optical Problem; Optical Problem
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16981507 ↗MalfunctionMay 22, 2023Optical Problem; Optical Problem
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16981479 ↗MalfunctionOct 31, 2022Poor Quality Image; Optical Problem; Optical Problem
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15700553 ↗MalfunctionSep 30, 2022Poor Quality Image
IT REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15512168 ↗
Other Laparoscope, general & plastic surgery devices
- HIGH DEFINITION LCD MONITOR OEV262HOlympus Medical Systems Corp. · Laparoscope, general & plastic surgery1,937 reports
- HD AUTOCLAVABLE CAMERA HEAD OTV-S7ProH-HD-12EOlympus Medical Systems Corp. · Laparoscope, general & plastic surgery1,886 reports
- HD AUTOCLAVABLE CAMERA HEAD OTV-S7ProH-HD-10EOlympus Medical Systems Corp. · Laparoscope, general & plastic surgery1,086 reports
- Auto Suture OMS-T10BTCovidien LP · Laparoscope, general & plastic surgery1 recall955 reports
- PDB OMS-PDB1000Covidien LP · Laparoscope, general & plastic surgery859 reports
- VISERA 4K UHD CAMERA CONTROL UNIT OLYMPUS OTV-S400Olympus Medical Systems Corp. · Laparoscope, general & plastic surgery777 reports
- Auto Suture OMS-T10SBCovidien LP · Laparoscope, general & plastic surgery1 recall697 reports
- Spacemaker SMBTTRNDXCovidien LP · Laparoscope, general & plastic surgery590 reports
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.
How reports and recalls are matched · Editorial policy · Report an error on this page