MICRORAPTOR 72205267Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00885556736234), received between Dec 9, 2020 and Dec 7, 2021 — classified as 2 injuries.

The most frequently reported specific device problem is “Flaked” (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.

• InjuryDec 7, 2021Flaked; Flaked

  IT WAS REPORTED THAT, DURING A DISLOCATION SURGERY A DRILL MICRORAPTOR HARD BONE WAS USED, WHILE DRILLING THE DEVICE GENERATED METAL POWDER, PART OF THE MATERIAL WAS REMOVED WITH SUCTION, BUT THE METAL POWDER COULD NOT BE COMPLETELY REMOVED FROM THE PATIENT. THE PROCEDURE WAS SUCCESSFULLY COMPLETED. A DELAY OF 10 MINUTES WAS REPORTED. A COMPETITOR DEVICE WAS USED. NO FURTHER COMPLICATIONS WERE REPORTED.

  Patient problems: Foreign Body In Patient; No Clinical Signs, Symptoms or Conditions

  MAUDE report 12952124 ↗
• InjuryDec 9, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT WHILE IN A CLINICAL STUDY USING DRILL MICRORAPTOR HARD BONE, THE PATIENT SUFFERED A RIGHT HIP LOCKING. AN MRI WAS PRESCRIBED TO THE PATIENT AND THE OUTCOME OF THE PATIENT IS UNKNOWN AT THE MOMENT. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED ACCORDINGLY.

  Patient problems: Reaction to Medicinal Component of Device

  MAUDE report 10979674 ↗