Precision Ideal Eyes 0502503030Recalls & reported problems
Stryker Corporation · HD Laparoscope, Autoclavable, 30 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 HD laparoscope is a reusable scope for general and plastic surgery. The 56 reports mostly describe image problems — blurry or fogged views during surgery — plus a few cases where parts of the scope broke or chipped, sometimes leaving a small fragment that was retrieved. Reports describe no deaths and no injuries. 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
- 59
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 59 adverse event reports that list this exact device (DI 07613327059144), received between Sep 11, 2019 and Sep 30, 2026 — classified as 59 malfunctions.
The most frequently reported specific device problem is “Poor Quality Image” (33 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 Image33
- Optical Problem19
- Fogging11
- Break5
- Nonstandard Device5
- Material Fragmentation4
- Moisture or Humidity Problem3
- Material Integrity Problem2
Patient problems
- No Clinical Signs, Symptoms or Conditions52
- Insufficient Information22
- No Known Impact Or Consequence To Patient7
- Abrasion1
- Burn(s)1
Recent adverse event reports
The 25 most recent of 59 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50952911 ↗MalfunctionSep 29, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50940525 ↗MalfunctionAug 26, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50462049 ↗MalfunctionJul 15, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25833916 ↗MalfunctionJan 8, 2026Material Fragmentation
IT WAS REPORTED THAT PIECE OF THE SCOPE IS BROKEN OFF. THEY REFERENCED THE DEVICE AS BROKEN AND ONLY A VERY SMALL PORTION OF THE DISTAL TIP WAS CHIPPED AND DETACHED INTO THE TROCAR. THEY BELIEVE THAT THE SCOPE MAY HAVE BEEN DROPPED DURING TRANSPORT. THIS ISSUE WAS IDENTIFIED AT ENTRY. THE DETACHED PIECE WAS SUCCESSFULLY RETRIEVED, AND A REPLACEMENT SCOPE WAS USED TO COMPLETE THE PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24004908 ↗MalfunctionNov 21, 2025Fogging; Fogging
IT WAS REPORTED THAT THERE WAS FOGGING ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23619843 ↗MalfunctionAug 20, 2025Fogging; Optical Problem; Fogging; Optical Problem
IT WAS REPORTED THAT THERE WAS FOGGY IMAGE DURING SURGERY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22854880 ↗MalfunctionApr 22, 2025Fogging; Moisture or Humidity Problem; Fogging; Moisture or Humidity Problem
IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21886356 ↗MalfunctionNov 8, 2024Fogging; Moisture or Humidity Problem; Fogging; Moisture or Humidity Problem
IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20645586 ↗MalfunctionNov 8, 2024Fogging; Moisture or Humidity Problem; Fogging; Moisture or Humidity Problem
IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20644931 ↗MalfunctionOct 24, 2024Break; Material Fragmentation; Break; Material Fragmentation
IT WAS REPORTED THAT THE DEVICE BROKE. PLEASE NOTE THAT THE BROKEN PIECE WAS SUCCESSFULLY REMOVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20522426 ↗MalfunctionJan 17, 2024Fracture; Detachment of Device or Device Component; Fracture; Detachment of Device or Device Component
IT WAS REPORTED THAT THE DEVICE BROKE. PLEASE NOTE THAT THE BROKEN PIECE WAS SUCCESSFULLY REMOVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18531188 ↗MalfunctionOct 12, 2023Fogging; Fogging
IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17926211 ↗MalfunctionSep 6, 2023Material Fragmentation; Material Integrity Problem; Material Fragmentation; Material Integrity Problem
IT WAS REPORTED THAT THE TIP OF THE SCOPE BROKE. THE BROKEN PIECE WAS SUCCESSFULLY REMOVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17694973 ↗MalfunctionSep 6, 2023Material Fragmentation; Material Integrity Problem; Material Fragmentation; Material Integrity Problem
IT WAS REPORTED THAT THE TIP OF THE SCOPE BROKE. THE BROKEN PIECE WAS SUCCESSFULLY REMOVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17694972 ↗MalfunctionAug 15, 2023Poor Quality Image; Poor Quality Image
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17553149 ↗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 17493739 ↗MalfunctionMay 25, 2023Optical Problem; Optical Problem
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17007932 ↗MalfunctionApr 27, 2023Sharp Edges; Sharp Edges
IT WAS REPORTED THAT THE PATIENT WAS SCRATCHED BY THE SHARP DISTAL TIP.
Patient problems: Abrasion
MAUDE report 16827490 ↗MalfunctionApr 21, 2023Optical Problem; Optical Problem
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE DURING PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16792209 ↗MalfunctionMar 13, 2023Poor Quality Image
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE DURING PROCEDURE.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 16527416 ↗MalfunctionJan 30, 2023Fogging; Poor Quality Image; Fogging
IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 16264711 ↗MalfunctionJan 5, 2023Poor Quality Image
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16104489 ↗MalfunctionDec 15, 2022Optical Problem; Optical Problem
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 15989080 ↗MalfunctionNov 23, 2022Poor Quality Image
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE DURING PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15858930 ↗
Other Laparoscope, general & plastic surgery devices
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- 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
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- 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.
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