N/A 72200917Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00885554012910), received between Sep 25, 2020 and May 8, 2021 — classified as 6 malfunctions.

The most frequently reported specific device problem is “Unstable” (4 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 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 8, 2021Unstable; Connection Problem; Unstable; Connection Problem

  IT WAS REPORTED THAT THE SPIDER FOR JAPANESE/ESCHMANN OR TABLE COULD NOT FIXED PROPERLY AND HAD A QUICK CONNECTOR FAILURE. NO CASE REPORTED; THEREFORE, NO PATIENT WAS INVOLVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11795353 ↗
• MalfunctionMar 31, 2021Unstable; Unstable

  IT WAS REPORTED THAT THE SPIDER'S FIXATION OF ARMS WAS LOOSE. NO CASE REPORTED; THEREFORE, THERE WAS NO PATIENT INVOLVEMENT. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED ACCORDINGLY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11599159 ↗
• MalfunctionFeb 6, 2021Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT THE SPIDER FOR JAPANESE/ESCHMANN OR TABLE HAD AN OIL LEAK. NO CASE REPORTED; THEREFORE, THERE WAS NO PATIENT INVOLVEMENT. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED ACCORDINGLY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11290303 ↗
• MalfunctionJan 30, 2021Unstable; Unstable

  IT WAS REPORTED THAT THE SPIDER 2 TENET ARM CANNOT BE FIXED. THE INCIDENT OCCURRED BEFORE THE PROCEDURE; NO DELAY WAS REPORTED. NO COMPLICATIONS WERE REPORTED. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED ACCORDINGLY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11256332 ↗
• MalfunctionDec 30, 2020Unstable; Unstable

  IT WAS REPORTED THAT THE SPIDER'S ARM WAS LOOSE. NO CASE REPORTED; THEREFORE, THERE WAS NO PATIENT INVOLVEMENT. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED ACCORDINGLY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11096186 ↗
• MalfunctionSep 25, 2020Positioning Problem; Positioning Problem

  IT WAS REPORTED THAT THE FIXATION OF SPIDER ARM WAS LOOSE. NO CASE INVOLVED. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED ACCORDINGLY.

  Patient problems: No Patient Involvement

  MAUDE report 10589819 ↗