Astra Tech Implant System® 22520Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 07392532002052), received between Jan 21, 2026 and Jul 7, 2026 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Mechanical Problem” (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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 7, 2026Mechanical Problem

  IT WAS REPORTED THAT THE IMPLANT DRIVER SHAFT BECAME STUCK INSIDE THE EXTENSION, AND THE DRILL EXTENSION SHAFT BECAME STUCK INSIDE THE HANDPIECE. NO INJURY RESULTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25737114 ↗
• MalfunctionJun 23, 2026Mechanical Problem

  IT WAS REPORTED THAT THERE WAS A TOOL ISSUE: THE IMPLANT DRIVER PEEK WAS STUCK. NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25594417 ↗
• MalfunctionApr 8, 2026Mechanical Problem

  CUSTOMER REPORTED THE TOOL ISSUE: THE IMPLANT DRIVER CANNOT GET STUCK.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24815760 ↗
• MalfunctionFeb 7, 2026Mechanical Problem

  IT WAS REPORTED THAT A PATIENT EXPERIENCED A TOOL MALFUNCTION. IT DOES NOT HOLD THE IMPLANT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24285988 ↗
• MalfunctionJan 21, 2026Material Deformation

  CIT WAS REPORTED THAT A PATIENT EXPERIENCED SHAFT DEFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24128555 ↗