Precision 0700410105Recalls & reported problems

Summary

The FDA's MAUDE database contains 13 adverse event reports that list this exact device (DI 07613327137378), received between Jan 10, 2020 and Mar 14, 2024 — classified as 13 malfunctions.

The most frequently reported specific device problem is “Poor Quality Image” (7 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.

Most reported problems

Recent adverse event reports

The 13 most recent of 13 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 14, 2024Poor Quality Image; Poor Quality Image

  IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18908880 ↗
• MalfunctionFeb 22, 2024Poor Quality Image; Poor Quality Image

  IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18762326 ↗
• MalfunctionFeb 20, 2024Poor Quality Image; Poor Quality Image

  IT WAS REPORTED THAT THERE WAS DARK IMAGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18744247 ↗
• MalfunctionDec 6, 2023No Display/Image; No Display/Image

  IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18279257 ↗
• MalfunctionNov 22, 2023No Display/Image; Output Problem; No Display/Image; Output Problem

  IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18194916 ↗
• MalfunctionApr 6, 2023Output Problem; Output Problem

  IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16690536 ↗
• MalfunctionMar 3, 2023Poor Quality Image; Output Problem; Output Problem

  IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16479840 ↗
• MalfunctionJun 21, 2022Poor Quality Image; Poor Quality Image

  IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14755291 ↗
• MalfunctionJun 2, 2022Poor Quality Image

  IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.

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

  MAUDE report 14574334 ↗
• MalfunctionJan 11, 2022Poor Quality Image

  IT WAS REPORTED THAT THERE WAS A BLURRY IMAGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13233285 ↗
• MalfunctionSep 13, 2021No Display/Image

  IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE DURING THE PROCEDURE.

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

  MAUDE report 12461412 ↗
• MalfunctionJun 10, 2021No Display/Image

  IT WAS REPORTED THERE WAS IMAGE LOSS FOR 3 MINUTES.

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

  MAUDE report 11977912 ↗
• MalfunctionJan 10, 2020Overheating of Device

  IT WAS REPORTED THAT A CAMERA HEAD WAS GETTING HOT.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9578297 ↗