SIDEKICK® SD110ATGRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741124884), received between Feb 2, 2021 and Apr 7, 2022 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (1 report).

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 16, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 7, 2022Retraction Problem; Device-Device Incompatibility; Material Deformation; Retraction Problem; Device-Device Incompatibility; Material Deformation

  IT WAS REPORTED THAT DURING A RECANALIZATION PROCEDURE VIA SUPERFICIAL FEMORAL ARTERY , THE CATHETER ALLEGEDLY HAD INCOMPATIBILITY ISSUE AND RETRACTION ISSUE. IT WAS FURTHER REPORTED THAT THE DEVICE WAS ALLEGEDLY DEFORMED. THE CATHETER AND WIRE REMOVED AS A SINGLE UNIT AND LOST WIRE ACCESS. THE PROCEDURE WAS COMPLETED USING ANOTHER DEVICE. THERE WAS NO REPORTED PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14038229 ↗
• MalfunctionFeb 2, 2021Break; Adverse Event Without Identified Device or Use Problem; Break; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT DURING A RECANALIZATION PROCEDURE, THE DISTAL END OF THE WIRE ALLEGEDLY BROKE OFF. IT WAS FURTHER REPORTED THAT THE BROKEN WIRE WAS REMOVED. THERE WAS NO REPORTED PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11264377 ↗