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1688 1688020122Recalls & reported problems

Stryker Corporation · Class 2

Adverse event reports
18
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 18 adverse event reports that list this exact device (DI 07613327382389), received between Jul 14, 2020 and Aug 31, 2026 — classified as 18 malfunctions.

The most frequently reported specific device problem is “Poor Quality Image” (11 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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 2 reportsFeb 2024: 1 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 3 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 1 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 2 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520263
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Poor Quality Image11
  • Fogging5
  • Moisture or Humidity Problem2
  • No Display/Image2
  • Image Orientation Incorrect1
  • Material Integrity Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions16
  • Insufficient Information3
  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 18 most recent of 18 reports, in the reporter's own words as published by the FDA.

  • MalfunctionAug 31, 2026Poor Quality Image

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50526572 ↗
  • MalfunctionAug 11, 2026Poor Quality Image

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50216342 ↗
  • MalfunctionApr 2, 2026Image Orientation Incorrect

    IT WAS REPORTED THAT THE REFLECTION OF THE CAMERA IMAGE INSIDE THE ABDOMEN IS FUNCTIONING AS A MIRROR. THEREFORE THE IMAGE ORIENTATION IS INCORRECT. THE MEDICAL PROCEDURE WAS ABORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24766320 ↗
  • MalfunctionJan 15, 2025Fogging; Fogging

    IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.

    Patient problems: Insufficient Information

    MAUDE report 21162270 ↗
  • MalfunctionJan 2, 2025Poor Quality Image; Poor Quality Image

    IT WAS REPORTED THAT THERE WAS POOR IMAGE QUALITY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21061228 ↗
  • MalfunctionJan 2, 2025Poor Quality Image; Poor Quality Image

    IT WAS REPORTED THAT THERE WAS POOR QUALITY IMAGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21061212 ↗
  • MalfunctionFeb 29, 2024Fogging; Fogging

    IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18813214 ↗
  • MalfunctionJan 24, 2024Poor Quality Image; Poor Quality Image

    IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18576408 ↗
  • MalfunctionJan 17, 2024Poor Quality Image; Poor Quality Image

    IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18530810 ↗
  • MalfunctionOct 27, 2023Poor Quality Image; Poor Quality Image

    IT WAS REPORTED THAT THERE WAS POOR IMAGE QUALITY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18025323 ↗
  • MalfunctionOct 27, 2023Poor Quality Image; Poor Quality Image

    IT WAS REPORTED THAT THERE WAS POOR IMAGE QUALITY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18025322 ↗
  • MalfunctionAug 23, 2023Fogging; 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 17602718 ↗
  • MalfunctionAug 21, 2023Fogging; 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 17584515 ↗
  • MalfunctionJan 19, 2023Poor Quality Image

    IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.

    Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions

    MAUDE report 16206301 ↗
  • MalfunctionMar 15, 2022Poor Quality Image

    IT WAS REPORTED THAT THERE WAS A POTENTIAL FOR ADVERSE CONSEQUENCES DUE TO BLURRY IMAGE.

    Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions

    MAUDE report 13772994 ↗
  • MalfunctionJan 11, 2022Material Integrity Problem; No Display/Image; Material Integrity Problem

    IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13227469 ↗
  • MalfunctionNov 22, 2021No Display/Image; No Display/Image

    IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12858188 ↗
  • MalfunctionJul 14, 2020Fogging; Poor Quality Image; Fogging; Poor Quality Image

    IT WAS REPORTED THAT THERE WAS AN UNCLEAR IMAGE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 10273932 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.