Watson Extraction System 17301Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00197169173017), received between Mar 3, 2026 and Mar 3, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Break” (3 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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 3, 2026Break; Device-Device Incompatibility

  IT WAS REPORTED THAT USED WATSON EXTRACTION SYSTEM TO REMOVE STEM WITH STRIKE PLATE ATTACHMENT. THE SLIDE HAMMER GOT STUCK OM THE EXTRACTOR HANDLE ONCE THE THREADED T HANDLE BROKE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24495135 ↗
• MalfunctionMar 3, 2026Break; Device-Device Incompatibility

  IT WAS REPORTED THAT USED WATSON EXTRACTION SYSTEM TO REMOVE STEM WITH STRIKE PLATE ATTACHMENT. THE SLIDE HAMMER GOT STUCK ON THE EXTRACTOR HANDLE ONCE THE THREADED T HANDLE BROKE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24495134 ↗
• MalfunctionMar 3, 2026Break; Device-Device Incompatibility

  IT WAS REPORTED THAT USED WATSON EXTRACTION SYSTEM TO REMOVE STEM WITH STRIKE PLATE ATTACHMENT. THE SLIDE HAMMER GOT STUCK OM THE EXTRACTOR HANDLE ONCE THE THREADED T HANDLE BROKE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24495133 ↗